A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977618



Internal ID19239080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:64347239..64400224hg38UCSC Ensembl
Outerchr9:43102900..43155900hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3852986
hg1953001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1115809
Supporting Variants
SamplesKWS2
Known GenesANKRD20A2, ANKRD20A3, LOC642929
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977618
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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