A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13698316



Internal ID21220165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108164015..108164015hg38UCSC Ensembl
chr7:107804460..107804460hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2814687
Supporting Variants
Samples
Known GenesNRCAM
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13698316
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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