A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714758



Internal ID138424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76952974..76952974hg38UCSC Ensembl
chr17:74949056..74949056hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5536145
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714758
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.15839


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