A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504003



Internal ID20877261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1720638..1729265hg38UCSC Ensembl
chr17:1623932..1632559hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg388628
hg198628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034086
Samples
Known GenesWDR81
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504003
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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