A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353701



Internal ID21011254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:143471396..143482174hg38UCSC Ensembl
chr2:144228965..144239743hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3810779
hg1910779
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18078067
Samples
Known GenesARHGAP15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353701
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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