A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060413



Internal ID20627453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31937201..31938600hg38UCSC Ensembl
chr1:32402802..32404201hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6325868
Supporting Variants
Samples
Known GenesPTP4A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060413
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.08118


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