A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1128501



Internal ID18919644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:86093583..86093633hg38UCSC Ensembl
Outerchr9:88708498..88708548hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960384
SamplesKWS1
Known GenesGOLM1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1128501
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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