A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610486



Internal ID20983557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131819715..131840499hg38UCSC Ensembl
chr6:132140855..132161639hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3820785
hg1920785
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215571
Samples
Known GenesENPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610486
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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