A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341300



Internal ID20998853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:190968873..190969496hg38UCSC Ensembl
chr2:191833599..191834222hg19UCSC Ensembl
Cytoband2q32.2
Allele length
AssemblyAllele length
hg38624
hg19624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083854
Samples
Known GenesSTAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341300
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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