A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977634



Internal ID18887792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:63767866..63844166hg38UCSC Ensembl
Outerchr9:68363600..68439900hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3876301
hg1976301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1115825
Supporting Variants
SamplesKWS2
Known GenesLOC642236
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977634
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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