A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv895369



Internal ID6302380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:49420008..50863623hg19UCSC Ensembl
Outerchr10:49410677..50868725hg19UCSC Ensembl
Innerchr10:49090014..50533629hg18UCSC Ensembl
Outerchr10:49080683..50538731hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1531614
SamplesMS10567
Known GenesARHGAP22, C10orf128, C10orf71, CHAT, DRGX, ERCC6, FAM170B, FRMPD2, LOC100506733, LRRC18, MAPK8, MIR4294, PGBD3, SLC18A3, VSTM4, WDFY4
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv895369
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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