A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512591



Internal ID20885927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35851083..35857476hg38UCSC Ensembl
chr17:34178087..34184480hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg386394
hg196394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035139
Samples
Known GenesC17orf66
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512591
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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