A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352543



Internal ID21010096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:236418039..236425111hg38UCSC Ensembl
chr2:237326682..237333754hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg387073
hg197073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087436
Samples
Known GenesIQCA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352543
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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