A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504793



Internal ID20878056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35236401..35243700hg38UCSC Ensembl
chr15:35528602..35535901hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg387300
hg197300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023375
Samples
Known GenesANP32AP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504793
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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