A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009703



Internal ID21919046
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 StatusM
Merged Variants
Supporting Variantsnssv17561865
Samples
Known GenesHCG4, HLA-G, HLA-H, LOC554223
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009703
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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