A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv889476



Internal ID6296487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:150730712..150944124hg19UCSC Ensembl
Outerchr7:150729212..150951819hg19UCSC Ensembl
Innerchr7:150361645..150575057hg18UCSC Ensembl
Outerchr7:150360145..150582752hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1549733
SamplesMS18276
Known GenesABCB8, ABCF2, ACCN3, AGAP3, ASB10, CDK5, CHPF2, FASTK, GBX1, MIR671, SLC4A2, SMARCD3, TMUB1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv889476
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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