A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458535



Internal ID21116088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:33138801..33156200hg38UCSC Ensembl
chr12:33291735..33309134hg19UCSC Ensembl
Cytoband12p11.1
Allele length
AssemblyAllele length
hg3817400
hg1917400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1488n223
Supporting Variantsnssv18000813
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458535
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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