A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18088173



Internal ID20655213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:29538244..29539016hg38UCSC Ensembl
chr2:29761110..29761882hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg38773
hg19773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6340667
Supporting Variants
Samples
Known GenesALK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18088173
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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