A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475335



Internal ID21132888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:65630732..65636143hg38UCSC Ensembl
chr12:66024512..66029923hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg385412
hg195412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18003015
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475335
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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