A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335781



Internal ID20993334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:181910297..181910667hg38UCSC Ensembl
chr2:182775024..182775394hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080990
Samples
Known GenesSSFA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335781
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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