A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137653



Internal ID19277988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:67450258..67480801hg38UCSC Ensembl
Outerchr9:65814900..65849300hg19UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3830544
hg1934401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3990154
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137653
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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