A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2815943



Internal ID21261281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:152674761..152674761hg38UCSC Ensembl
chr7:152371846..152371846hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13705961
Samples
Known GenesXRCC2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2815943
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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