A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17574827



Internal ID21766870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:41919434..41919434hg38UCSC Ensembl
chr7:41959032..41959032hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6065719
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17574827
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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