A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951732



Internal ID16953919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:40208883..40223482hg38UCSC Ensembl
Outerchr9:42353901..42368500hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3814600
hg1914600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999421
SamplesBILGI_BIOE
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951732
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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