A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132276



Internal ID18930592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:2652061..2700461hg38UCSC Ensembl
Outerchr1:2583500..2631900hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3848401
hg1948401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv16n106
Supporting Variantsnssv3987043
SamplesKWS1
Known GenesTTC34
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132276
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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