A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17037511



Internal ID92763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72205672..72206329hg38UCSC Ensembl
chr10:73965430..73966087hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38658
hg19658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143234
Supporting Variants
Samples
Known GenesASCC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17037511
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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