A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv889471



Internal ID6296482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:150707488..150747746hg19UCSC Ensembl
Outerchr7:150700946..150751590hg19UCSC Ensembl
Innerchr7:150338421..150378679hg18UCSC Ensembl
Outerchr7:150331879..150382523hg18UCSC 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 Variantsnssv1543509
SamplesMS16153
Known GenesABCB8, ACCN3, ATG9B, CDK5, NOS3
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv889471
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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