A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17572601



Internal ID21764644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:53743638..53743765hg38UCSC Ensembl
chr6:53608436..53608563hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6006753
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17572601
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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