A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13699356



Internal ID21221200
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 StatusS
Merged Variantsnsv2802781
Supporting Variants
Samples
Known GenesLINC00029, LOC63930
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13699356
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.709677


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