A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2815999



Internal ID21261337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155367158..155367235hg38UCSC Ensembl
chr7:155159853..155159930hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13702579
Samples
Known GenesBLACE
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2815999
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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