A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv886539



Internal ID6293550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:111531412..111744319hg19UCSC Ensembl
Outerchr6:111526494..111744818hg19UCSC Ensembl
Innerchr6:111638105..111851012hg18UCSC Ensembl
Outerchr6:111633187..111851511hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1539800
SamplesMS14502
Known GenesKIAA1919, REV3L, SLC16A10
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv886539
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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