A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463619



Internal ID21121172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:81254401..81255200hg38UCSC Ensembl
chr12:81648180..81648979hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18003726
Samples
Known GenesACSS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463619
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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