A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3997313



Internal ID18844799
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 StatusS
Merged Variantsnsv1145949
Supporting Variants
SamplesKWB1
Known GenesTP73
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3997313
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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