A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343651



Internal ID21001204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68299509..68305427hg38UCSC Ensembl
chr2:68526641..68532559hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg385919
hg195919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088827
Samples
Known GenesCNRIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343651
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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