A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339695



Internal ID20997248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:71247286..71283230hg38UCSC Ensembl
chr2:71474416..71510360hg19UCSC Ensembl
Cytoband2p13.2
Allele length
AssemblyAllele length
hg3835945
hg1935945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089602
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339695
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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