A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110558



Internal ID19259599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:62907476..62933076hg38UCSC Ensembl
Outerchr9:66563300..66588900hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3825601
hg1925601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4028n106
Supporting Variantsnssv3960212
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110558
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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