A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007663



Internal ID21917006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73669792..73670952hg38UCSC Ensembl
chr10:75429550..75430710hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg381161
hg191161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586068
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007663
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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