A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504656



Internal ID20877919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80950061..80953849hg38UCSC Ensembl
chr15:81242402..81246190hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg383789
hg193789
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026441
Samples
Known GenesKIAA1199
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504656
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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