A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618309



Internal ID21810356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6772337..6772417hg38UCSC Ensembl
chr17:6675656..6675736hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036716
Supporting Variants
Samples
Known GenesXAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618309
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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