A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124450



Internal ID19274934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:93448405..93448462hg38UCSC Ensembl
Outerchr9:96210687..96210744hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3975747
SamplesKWS2
Known GenesFAM120AOS
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124450
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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