A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510963



Internal ID20884287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16753201..16844100hg38UCSC Ensembl
chr17:16656515..16747414hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3890900
hg1990900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3015n223
Supporting Variantsnssv18178768
Samples
Known GenesCCDC144A, FAM106CP, KRT16P2, USP32P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510963
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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