A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149505



Internal ID19196324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:25604079..25608780hg38UCSC Ensembl
Outerchr7:25643699..25648400hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg384702
hg194702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000807
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149505
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