A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2815176



Internal ID21260514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:51203207..51203476hg38UCSC Ensembl
chr7:51270904..51271173hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13707717
Samples
Known GenesCOBL
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2815176
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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