A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347546



Internal ID21005099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68829490..68839954hg38UCSC Ensembl
chr2:69056622..69067086hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg3810465
hg1910465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088862
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347546
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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