A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv883537



Internal ID6290548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29746657..29766926hg19UCSC Ensembl
Outerchr6:29746023..29767611hg19UCSC Ensembl
Innerchr6:29854636..29874905hg18UCSC Ensembl
Outerchr6:29854002..29875590hg18UCSC 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 Variantsnssv1556711
SamplesMS22122
Known GenesHCG4, LOC554223
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv883537
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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