A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv894855



Internal ID6301866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:8108290..8111168hg19UCSC Ensembl
Outerchr10:8106747..8111409hg19UCSC Ensembl
Innerchr10:8148296..8151174hg18UCSC Ensembl
Outerchr10:8146753..8151415hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1516269, nssv1519240
SamplesSP80988, SP56734
Known GenesGATA3
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv894855
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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