A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032851



Internal ID21942194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64018840..64018943hg38UCSC Ensembl
chr17:62096200..62096303hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628814
Samples
Known GenesICAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032851
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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