A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113019



Internal ID19260856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:130378213..130378713hg38UCSC Ensembl
Outerchr9:133253600..133254100hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4150n106
Supporting Variantsnssv3967905
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113019
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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