A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18002121



Internal ID20569161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:62898748..62908837hg38UCSC Ensembl
chr12:63292528..63302617hg19UCSC Ensembl
Cytoband12q14.2
Allele length
AssemblyAllele length
hg3810090
hg1910090
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462783
Supporting Variants
Samples
Known GenesPPM1H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18002121
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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