A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950999



Internal ID16953186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:97250644..97252143hg38UCSC Ensembl
Outerchr10:99010401..99011900hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998031
SamplesBILGI_BIOE
Known GenesARHGAP19, ARHGAP19-SLIT1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950999
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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