A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407975



Internal ID21065528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36253033..36383991hg38UCSC Ensembl
chr6:36220810..36351768hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38130959
hg19130959
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231740
Samples
Known GenesC6orf222, ETV7, PNPLA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407975
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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