A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18077900



Internal ID20644941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:135641209..135645279hg38UCSC Ensembl
chr2:136398779..136402849hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg384071
hg194071
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6353680
Supporting Variants
Samples
Known GenesR3HDM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18077900
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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