A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352929



Internal ID21010482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:188235306..188240446hg38UCSC Ensembl
chr2:189100033..189105173hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg385141
hg195141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081157
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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