A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132224



Internal ID19268290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:128184823..128184895hg38UCSC Ensembl
Outerchr9:130947102..130947174hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3986969
SamplesKWS1
Known GenesCIZ1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132224
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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