A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346128



Internal ID21003681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:143640291..143640686hg38UCSC Ensembl
chr2:144397860..144398255hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18078082
Samples
Known GenesARHGAP15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346128
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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