A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951789



Internal ID17300663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:130880714..130963813hg38UCSC Ensembl
Outerchr9:133756101..133839200hg19UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg3883100
hg1983100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997001
SamplesBILGI_BIOE
Known GenesABL1, FIBCD1, QRFP
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951789
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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