A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504705



Internal ID20877968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67290785..67291173hg38UCSC Ensembl
chr15:67583123..67583511hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025448
Samples
Known GenesIQCH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504705
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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