A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18089473



Internal ID20656513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61412119..61414354hg38UCSC Ensembl
chr2:61639254..61641489hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg382236
hg192236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6339003
Supporting Variants
Samples
Known GenesUSP34
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18089473
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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