A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461603



Internal ID21119156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:94055631..94807220hg38UCSC Ensembl
chr12:94449407..95200996hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38751590
hg19751590
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186682
Samples
Known GenesCCDC41, CCDC41-AS1, MIR5700, MIR7844, PLXNC1, TMCC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461603
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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