A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460748



Internal ID21118301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:27007901..27009600hg38UCSC Ensembl
chr12:27160834..27162533hg19UCSC Ensembl
Cytoband12p11.23
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18000063
Samples
Known GenesTM7SF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460748
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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