A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17607883



Internal ID21799930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95080513..95080607hg38UCSC Ensembl
chr15:95623742..95623836hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6029636
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17607883
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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