A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469306



Internal ID21126859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:76868868..77024812hg38UCSC Ensembl
chr12:77262648..77418592hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg38155945
hg19155945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18004127
Samples
Known GenesCSRP2, E2F7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469306
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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