A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18088821



Internal ID20655861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68131261..68134163hg38UCSC Ensembl
chr2:68358393..68361295hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg382903
hg192903
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6353608
Supporting Variants
Samples
Known GenesWDR92
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18088821
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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