A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110576



Internal ID19258714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:68238684..68249784hg38UCSC Ensembl
Outerchr9:70853600..70864700hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3811101
hg1911101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960230
SamplesKWS1
Known GenesCBWD3, CBWD5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110576
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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