A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004649



Internal ID21913992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38286977..38287320hg38UCSC Ensembl
chr8:38144495..38144838hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576860
Samples
Known GenesWHSC1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004649
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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