A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499130



Internal ID20872347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22745801..22786400hg38UCSC Ensembl
chr15:23086668..23127305hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3840600
hg1940638
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2380n223
Supporting Variantsnssv18183905
Samples
Known GenesLOC283683, NIPA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499130
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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