A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16994213



Internal ID63598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25160253..25160260hg38UCSC Ensembl
chr7:25199872..25199879hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5533930
Supporting Variants
Samples
Known GenesC7orf31
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16994213
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.256947


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