A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17559061



Internal ID21883416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38337571..38337673hg38UCSC Ensembl
chr8:38195089..38195191hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6007569
Supporting Variants
Samples
Known GenesWHSC1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17559061
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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