A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511683



Internal ID20885013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21238775..21240825hg38UCSC Ensembl
chr17:21142088..21144138hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg382051
hg192051
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034301
Samples
Known GenesC17orf103
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511683
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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