A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351331



Internal ID21008884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:181308501..181315400hg38UCSC Ensembl
chr2:182173228..182180127hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg386900
hg196900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080935
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351331
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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