A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341250



Internal ID20998803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:236207975..236213954hg38UCSC Ensembl
chr2:237116618..237122597hg19UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg385980
hg195980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087431
Samples
Known GenesASB18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341250
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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