A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978315



Internal ID19242219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:63316828..63344528hg38UCSC Ensembl
Outerchr9:67271800..67299500hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3827701
hg1927701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1139979
Supporting Variants
SamplesKWS2
Known GenesAQP7P1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978315
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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