A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496003



Internal ID20869201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16613001..16622100hg38UCSC Ensembl
chr17:16516315..16525414hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg389100
hg199100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179220
Samples
Known GenesZNF624
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496003
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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