A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145949



Internal ID18854795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:3706442..3706528hg38UCSC Ensembl
Outerchr1:3623006..3623092hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997313
SamplesKWB1
Known GenesTP73
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1145949
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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