A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609100



Internal ID20982171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131790001..131825800hg38UCSC Ensembl
chr6:132111141..132146940hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3835800
hg1935800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6402n223
Supporting Variantsnssv18215569
Samples
Known GenesENPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609100
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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