A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502615



Internal ID20875861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1497271..1499336hg38UCSC Ensembl
chr17:1400565..1402630hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg382066
hg192066
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185921
Samples
Known GenesINPP5K
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502615
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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