A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463137



Internal ID21120690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50540723..50552407hg38UCSC Ensembl
chr12:50934506..50946190hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg3811685
hg1911685
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18001265
Samples
Known GenesDIP2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463137
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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