A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2802781



Internal ID21248119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63034892..63034963hg38UCSC Ensembl
chr20:61666244..61666315hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13699356
Samples
Known GenesLINC00029, LOC63930
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2802781
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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