A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv878328



Internal ID6285339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1147407..1986972hg19UCSC Ensembl
Outerchr4:1141573..1990425hg19UCSC Ensembl
Innerchr4:1137407..1956770hg18UCSC Ensembl
Outerchr4:1131573..1960223hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1546543
SamplesMS17208
Known GenesC4orf42, CRIPAK, CTBP1, FAM53A, FGFR3, KIAA1530, LETM1, LOC100130872, MAEA, MIR943, SCARNA22, SLBP, SPON2, TACC3, TMEM129, WHSC1, WHSC2
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv878328
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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