A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415531



Internal ID21073084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29819360..29935382hg38UCSC Ensembl
chr6:29787137..29903159hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38116023
hg19116023
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6109n223
Supporting Variantsnssv18141388
Samples
Known GenesHCG4B, HLA-G, HLA-H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415531
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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