A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132981



Internal ID19248840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:74346447..74346497hg38UCSC Ensembl
Outerchr9:76961363..76961413hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3987775
SamplesKWS1
Known GenesMIR6130
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132981
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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