A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977866



Internal ID52635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1796147..1796263hg38UCSC Ensembl
chr6:1796381..1796497hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467634
Supporting Variants
Samples
Known GenesGMDS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977866
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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