A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2815639



Internal ID21260977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77725415..77725415hg38UCSC Ensembl
chr7:77354732..77354732hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13705233
Samples
Known GenesRSBN1L
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2815639
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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