A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032004



Internal ID89042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32501281..32502090hg38UCSC Ensembl
chr10:32790209..32791018hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38810
hg19810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488578
Supporting Variants
Samples
Known GenesCCDC7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032004
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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