A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068044



Internal ID20635084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36256702..36266576hg38UCSC Ensembl
chr20:34844624..34854498hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg389875
hg199875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526683
Supporting Variants
Samples
Known GenesAAR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068044
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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