A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3939687



Internal ID21359756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29629592..29630062hg38UCSC Ensembl
chr10:29918521..29918991hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38471
hg19471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15180958
SamplesHG002
Known GenesSVIL
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3939687
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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