A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353777



Internal ID21011330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231542563..231680403hg38UCSC Ensembl
chr2:232407274..232545113hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38137841
hg19137840
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206207
Samples
Known GenesC2orf57
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353777
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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