A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498113



Internal ID20871321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38517362..38946780hg38UCSC Ensembl
chr15:38809563..39238981hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38429419
hg19429419
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178706
Samples
Known GenesC15orf53, RASGRP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498113
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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