A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950957



Internal ID16953144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:46120422..46123621hg38UCSC Ensembl
Outerchr10:51472201..51475400hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997989
SamplesBILGI_BIOE
Known GenesAGAP7
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950957
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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