A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153740



Internal ID19198206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:27743816..27744108hg38UCSC Ensembl
Outerchr7:27783435..27783727hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002394
SamplesKWB1
Known GenesTAX1BP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153740
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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