A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18077626



Internal ID20644666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:134832114..134840325hg38UCSC Ensembl
chr2:135589684..135597895hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg388212
hg198212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6339571
Supporting Variants
Samples
Known GenesACMSD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18077626
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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