A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15180934



Internal ID21319730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18741447..18741597hg38UCSC Ensembl
chr10:19030376..19030526hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3933244
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15180934
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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