A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2815100



Internal ID21260438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108188805..108188805hg38UCSC Ensembl
chr7:107829249..107829249hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg386068
hg196068
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13705309
Samples
Known GenesNRCAM
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2815100
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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