A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339178



Internal ID20996731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:60465805..60470330hg38UCSC Ensembl
chr2:60692940..60697465hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg384526
hg194526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090594
Samples
Known GenesBCL11A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339178
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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