A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15180958



Internal ID21319754
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3939687
Supporting Variants
SamplesHG002
Known GenesSVIL
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15180958
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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