A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468627



Internal ID21126180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:68151812..68152523hg38UCSC Ensembl
chr12:68545592..68546303hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg38712
hg19712
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002694
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468627
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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