A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv883539



Internal ID6290550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29749292..29778987hg19UCSC Ensembl
Outerchr6:29748206..29780529hg19UCSC Ensembl
Innerchr6:29857271..29886966hg18UCSC Ensembl
Outerchr6:29856185..29888508hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1553347
SamplesMS19941
Known GenesHCG4, LOC554223
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv883539
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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