A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119567



Internal ID18938497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:112866926..112867009hg38UCSC Ensembl
Outerchr9:115629206..115629289hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960767
SamplesKWS1
Known GenesSNX30
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119567
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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