A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151399



Internal ID18849592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:16849404..16949205hg38UCSC Ensembl
Outerchr1:17175899..17275700hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3899802
hg1999802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003962
SamplesKWB1
Known GenesCROCC, MIR3675
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151399
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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