A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2817464



Internal ID21262802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87380367..87380367hg38UCSC Ensembl
chr7:87009683..87009683hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13708895
Samples
Known GenesCROT
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2817464
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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