A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463934



Internal ID21121487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:97639446..97667640hg38UCSC Ensembl
chr12:98033224..98061418hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3828195
hg1928195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006065
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463934
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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