A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17591200



Internal ID21783243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43138232..43138430hg38UCSC Ensembl
chr10:43633680..43633878hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6009496
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17591200
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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