A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460125



Internal ID21117678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92762607..92763347hg38UCSC Ensembl
chr12:93156383..93157123hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38741
hg19741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005786
Samples
Known GenesPLEKHG7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460125
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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