A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495982



Internal ID20869179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:23561301..23568300hg38UCSC Ensembl
chr15:23806448..23813447hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg387000
hg197000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177290
Samples
Known GenesMIR4508, MKRN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495982
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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