A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1139974



Internal ID19255710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:62907576..62927976hg38UCSC Ensembl
Outerchr9:66563400..66583800hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3820401
hg1920401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4028n106
Supporting Variantsnssv3978310
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1139974
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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