A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18005262



Internal ID20572302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:87815838..88090776hg38UCSC Ensembl
chr12:88209615..88484553hg19UCSC Ensembl
Cytoband12q21.32
Allele length
AssemblyAllele length
hg38274939
hg19274939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466059
Supporting Variants
Samples
Known GenesC12orf29, C12orf50, CEP290
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18005262
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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