A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346481



Internal ID21004034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:69806684..69812065hg38UCSC Ensembl
chr2:70033816..70039197hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg385382
hg195382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088903
Samples
Known GenesANXA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346481
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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