A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18089273



Internal ID20656313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63938765..63983389hg38UCSC Ensembl
chr2:64165899..64210523hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3844625
hg1944625
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6340192
Supporting Variants
Samples
Known GenesVPS54
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18089273
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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