A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18075885



Internal ID20642925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:119639008..119656415hg38UCSC Ensembl
chr2:120396584..120413991hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg3817408
hg1917408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6348501
Supporting Variants
Samples
Known GenesPCDP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18075885
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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