A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608432



Internal ID21800479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66516635..66517860hg38UCSC Ensembl
chr15:66808973..66810198hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381226
hg191226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028568
Supporting Variants
Samples
Known GenesZWILCH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608432
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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