A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952727



Internal ID17301601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:143276001..143290084hg38UCSC Ensembl
Outerchr1:149020001..149035800hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg3814084
hg1915800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997300
SamplesBILGI_BIOE
Known GenesLOC101929780
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952727
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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