A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17573136



Internal ID21765179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:46310737..46310737hg38UCSC Ensembl
chr7:46350335..46350335hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg381007
hg191007
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6074252
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17573136
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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