A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471186



Internal ID21128739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:61805701..61817200hg38UCSC Ensembl
chr12:62199482..62210981hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg3811500
hg1911500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1556n223
Supporting Variantsnssv18002386
Samples
Known GenesFAM19A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471186
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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