A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137652



Internal ID18930004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:39057276..39077568hg38UCSC Ensembl
Outerchr9:65658300..65678600hg19UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3820293
hg1920301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3990153
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137652
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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