A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6348952



Internal ID21006505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:77915058..77993755hg38UCSC Ensembl
chr2:78142184..78220881hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3878698
hg1978698
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3933n223
Supporting Variantsnssv18207678
Samples
Known GenesSNAR-H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6348952
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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