A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476107



Internal ID21133660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109794479..109885546hg38UCSC Ensembl
chr12:110232284..110323351hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg3891068
hg1991068
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996881
Samples
Known GenesGLTP, MIR4497, TRPV4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476107
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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