A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953892



Internal ID17302766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:38457357..38513464hg38UCSC Ensembl
Outerchr17:36613601..36669700hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3856108
hg1956100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998738
SamplesBILGI_BIOE
Known GenesARHGAP23
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953892
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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