A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6307919



Internal ID9386642
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 Flag1
Merged StatusS
Merged Variantsesv2658586
Supporting Variants
SamplesNA18579
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6307919
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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