A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv888796



Internal ID6295807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:100342950..100422156hg19UCSC Ensembl
Outerchr7:100313420..100423365hg19UCSC Ensembl
Innerchr7:100180886..100260092hg18UCSC Ensembl
Outerchr7:100151356..100261301hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1538616
SamplesMS13770
Known GenesEPHB4, EPO, ZAN
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv888796
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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