A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662908



Internal ID9582327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96267537..96273699hg38UCSC Ensembl
chr13:96919791..96925953hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg386163
hg196163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv376e199
Supporting Variantsessv6287043, essv5751585, essv5555089, essv5749894, essv6400542, essv6393928, essv6546843, essv6460508
SamplesNA19904, NA18523, NA19311, NA18511, NA19467, NA18856, NA19190, NA19332
Known GenesHS6ST3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662908
Frequency
Sample Size1151
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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