A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518969



Internal ID20892330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:82181801..82461700hg38UCSC Ensembl
chr17:80139677..80419576hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38279900
hg19279900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195670
Samples
Known GenesC17orf62, CCDC57, CD7, CSNK1D, HEXDC, MIR6787, NARF, OGFOD3, SECTM1, SLC16A3, TEX19, UTS2R
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518969
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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