A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115822



Internal ID19286043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:63288428..63316328hg38UCSC Ensembl
Outerchr9:67243400..67271300hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3827901
hg1927901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3977631
SamplesKWS2
Known GenesAQP7P1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115822
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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