A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2794627



Internal ID21239965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73191320..73191503hg38UCSC Ensembl
chr15:73483661..73483844hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13702546
Samples
Known GenesNEO1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2794627
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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