A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657781



Internal ID9577200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132764490..132764867hg38UCSC Ensembl
chr10:134577994..134578371hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38378
hg19378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5672178, essv5625132, essv6149710, essv5849776, essv5781349, essv5853062, essv5570107, essv5468150, essv6554673, essv6545376, essv6015629, essv6176817, essv5942431
SamplesHG01083, NA19469, NA19455, HG01082, NA19463, HG01047, NA19703, NA19394, NA20518, NA19434, HG00608, NA19452, NA19746
Known GenesINPP5A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657781
Frequency
Sample Size1151
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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