A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032971



Internal ID89681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32912127..32919882hg38UCSC Ensembl
chr10:33201055..33208810hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg387756
hg197756
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147073
Supporting Variants
Samples
Known GenesITGB1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032971
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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