A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337994



Internal ID20995547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:119630566..119637230hg38UCSC Ensembl
chr2:120388142..120394806hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg386665
hg196665
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075884
Samples
Known GenesPCDP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337994
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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