A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13677290



Internal ID21199142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67709906..67710059hg38UCSC Ensembl
chr1:68175589..68175742hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2802569
Supporting Variants
Samples
Known GenesGNG12
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13677290
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.578125


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