A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464932



Internal ID21122485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:22495162..22495920hg38UCSC Ensembl
chr12:22648096..22648854hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38759
hg19759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17998344
Samples
Known GenesC2CD5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464932
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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