A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396200



Internal ID21053753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36778369..36862136hg38UCSC Ensembl
chr6:36746146..36829912hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3883768
hg1983767
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219997
Samples
Known GenesCPNE5, PPIL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396200
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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