A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv889477



Internal ID6296488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:150732463..150832913hg19UCSC Ensembl
Outerchr7:150731698..150837529hg19UCSC Ensembl
Innerchr7:150363396..150463846hg18UCSC Ensembl
Outerchr7:150362631..150468462hg18UCSC 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 Variantsnssv1546642
SamplesMS17208
Known GenesABCB8, ACCN3, AGAP3, CDK5, FASTK, SLC4A2, TMUB1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv889477
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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