A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151591



Internal ID18854557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:183018035..183018115hg38UCSC Ensembl
Outerchr3:182735823..182735903hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003014
SamplesKWB1
Known GenesMCCC1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151591
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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