A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501767



Internal ID20875004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45487467..45491836hg38UCSC Ensembl
chr15:45779665..45784034hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg384370
hg194370
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024612
Samples
Known GenesSLC30A4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501767
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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