A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952774



Internal ID17301648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:149681918..149689124hg38UCSC Ensembl
Outerchr1:149653501..149660700hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg387207
hg197200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997312
SamplesBILGI_BIOE
Known GenesLINC00869
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952774
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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