A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129001



Internal ID19252749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:64455114..64476244hg38UCSC Ensembl
Outerchr9:43020700..43041800hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3821131
hg1921101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4004n106
Supporting Variantsnssv3961673
SamplesKWS1
Known GenesFAM95B1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129001
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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