A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18077922



Internal ID20644963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:136166780..136168135hg38UCSC Ensembl
chr2:136924350..136925705hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg381356
hg191356
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6345410
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18077922
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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