A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv958449



Internal ID17307322
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 StatusM
Merged Variants
Supporting Variantsnssv3001029
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv958449
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer