A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021244



Internal ID21930587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38631111..38631245hg38UCSC Ensembl
chr17:36787364..36787498hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628808
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021244
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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