A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347860



Internal ID21005413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:6906401..6912400hg38UCSC Ensembl
chr2:7046532..7052531hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088873
Samples
Known GenesRNF144A-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347860
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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