A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18075077



Internal ID20642117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:103953008..103953799hg38UCSC Ensembl
chr2:104569466..104570257hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg38792
hg19792
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6349628
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18075077
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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