A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035496



Internal ID21944839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72236544..72236865hg38UCSC Ensembl
chr17:70232685..70233006hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632677
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035496
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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