A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658586



Internal ID9924691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155386878..155387021hg38UCSC Ensembl
chr7:155179573..155179716hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5835905, essv6263759, essv6052264, essv6033671, essv5515056, essv6572222, essv6492006, essv6435546, essv5629254, essv5894381, essv6014249, essv6502737, essv5982519, essv5947165, essv5979240, essv5823847, essv5619139, essv6156458, essv5414346, essv6388702, essv6231804, essv5596223, essv5856766, essv6102933, essv6261849, essv6259678, essv6213270, essv6307919, essv5928945, essv6585589, essv5669694, essv5451668
SamplesNA18502, NA11830, NA12414, NA19355, NA18526, NA19374, NA19373, NA19313, NA19138, NA18874, NA11994, NA19172, NA18520, NA11831, NA19403, NA18516, NA18579, NA11919, NA19099, NA19257, NA18523, NA18953, NA19390, NA19835, NA19398, NA19328, NA19468, NA19713, HG01254, NA19102, HG01082, NA12776
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658586
Frequency
Sample Size1151
Observed Gain0
Observed Loss32
Observed Complex0
Frequencyn/a


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