A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136180



Internal ID18910474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:174225897..174226217hg38UCSC Ensembl
Outerchr2:175090625..175090945hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2096n106
Supporting Variantsnssv3989790
SamplesKWS1
Known GenesOLA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136180
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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