A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17562079



Internal ID21886434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39740288..39740288hg38UCSC Ensembl
chr7:39779887..39779887hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38929
hg19929
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6068373
Supporting Variants
Samples
Known GenesLINC00265
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17562079
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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