A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002649



Internal ID21911992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96533535..96533735hg38UCSC Ensembl
chr8:97545763..97545963hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592564
Samples
Known GenesSDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002649
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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