A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136460



Internal ID18920225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:195740600..195740656hg38UCSC Ensembl
Outerchr2:196605324..196605380hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3972847
SamplesKWS2
Known GenesDNAH7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136460
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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