A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460736



Internal ID21118289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8656793..8659364hg38UCSC Ensembl
chr12:8809389..8811960hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg382572
hg192572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005471
Samples
Known GenesMFAP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460736
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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