A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396295



Internal ID21053848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:72121730..72160461hg38UCSC Ensembl
chr6:72831433..72870164hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3838732
hg1938732
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218872
Samples
Known GenesRIMS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396295
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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