A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190858



Internal ID20757898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35209801..35252400hg38UCSC Ensembl
chr15:35502002..35544601hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3842600
hg1942600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497617
Supporting Variants
Samples
Known GenesANP32AP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190858
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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