A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17587683



Internal ID21779726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70985200..70985303hg38UCSC Ensembl
chr10:72744957..72745060hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6008327
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17587683
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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