A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032961



Internal ID89672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32820668..32869828hg38UCSC Ensembl
chr10:33109596..33158756hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3849161
hg1949161
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147423
Supporting Variants
Samples
Known GenesCCDC7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032961
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.133625


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