A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126874



Internal ID18915153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:39184503..39296503hg38UCSC Ensembl
Outerchr9:39184500..39296500hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38112001
hg19112001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3985151
SamplesKWS1
Known GenesCNTNAP3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126874
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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