A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335903



Internal ID20993456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:144312498..144324481hg38UCSC Ensembl
chr2:145070065..145082048hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3811984
hg1911984
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207300
Samples
Known GenesGTDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335903
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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