A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417355



Internal ID21074908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:20638743..20651304hg38UCSC Ensembl
chr9:20638742..20651303hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3812562
hg1912562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175890
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417355
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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