A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18000006



Internal ID20567046
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 StatusS
Merged Variantsnsv6469908
Supporting Variants
Samples
Known GenesRASSF8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18000006
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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