A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3001029



Internal ID17293981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:105908650..105908808hg38UCSC Ensembl
Outerchr7:105549096..105549254hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv958449
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3001029
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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