A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2815599



Internal ID21260937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:152674741..152674741hg38UCSC Ensembl
chr7:152371826..152371826hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13703976
Samples
Known GenesXRCC2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2815599
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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