A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17561865



Internal ID21886220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29771078..29918287hg38UCSC Ensembl
chr6:29738855..29886064hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38147210
hg19147210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6009703
Supporting Variants
Samples
Known GenesHCG4, HLA-G, HLA-H, LOC554223
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17561865
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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