A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499479



Internal ID20872699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100442958..101075208hg38UCSC Ensembl
chr15:100983163..101615413hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38632251
hg19632251
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183432
Samples
Known GenesALDH1A3, ASB7, CERS3, LINS, LRRK1, PRKXP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499479
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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