A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469908



Internal ID21127461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:26031367..26032050hg38UCSC Ensembl
chr12:26184300..26184983hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38684
hg19684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18000006
Samples
Known GenesRASSF8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469908
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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