A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950952



Internal ID16953139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:48445358..48458757hg38UCSC Ensembl
Outerchr10:49653401..49666800hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3813400
hg1913400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997984
SamplesBILGI_BIOE
Known GenesARHGAP22
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950952
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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