A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455911



Internal ID21113464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:53311487..53312785hg38UCSC Ensembl
chr12:53705271..53706569hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg381299
hg191299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18001444
Samples
Known GenesAAAS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455911
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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