A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977650



Internal ID18883836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:101596818..101599718hg38UCSC Ensembl
Outerchr9:104359100..104362000hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg382901
hg192901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1115841
Supporting Variants
SamplesKWS2
Known GenesGRIN3A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977650
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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