A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477813



Internal ID21135366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122774401..122774800hg38UCSC Ensembl
chr12:123258948..123259347hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17998749
Samples
Known GenesCCDC62
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477813
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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