A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv880970



Internal ID6287981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:175434520..175443156hg19UCSC Ensembl
Outerchr4:175434394..175444006hg19UCSC Ensembl
Innerchr4:175671095..175679731hg18UCSC Ensembl
Outerchr4:175670969..175680581hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1507269
SamplesSP54516
Known GenesHPGD
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv880970
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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