A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355482



Internal ID21013035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:191130355..191133929hg38UCSC Ensembl
chr2:191995081..191998655hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg383575
hg193575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083856
Samples
Known GenesSTAT4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355482
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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