A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv895365



Internal ID6302376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:49295316..51122366hg19UCSC Ensembl
Outerchr10:49246290..51127510hg19UCSC Ensembl
Innerchr10:48965322..50792372hg18UCSC Ensembl
Outerchr10:48916296..50797516hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1525241
SamplesSP56377
Known GenesARHGAP22, C10orf128, C10orf53, C10orf71, CHAT, DRGX, ERCC6, FAM170B, FRMPD2, FRMPD2P1, LOC100506733, LRRC18, MAPK8, MIR4294, OGDHL, PARG, PGBD3, SLC18A3, VSTM4, WDFY4
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv895365
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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