A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3993125



Internal ID19235946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:62557199..62596899hg38UCSC Ensembl
Outerchr9:46868500..46908200hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3839701
hg1939701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1141620
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3993125
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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