A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351103



Internal ID21008656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:238386401..238390000hg38UCSC Ensembl
chr2:239295042..239298641hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084436
Samples
Known GenesTRAF3IP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351103
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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