A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997106



Internal ID16943372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:26698210..26706209hg38UCSC Ensembl
Outerchr1:27024701..27032700hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950341
Supporting Variants
SamplesBILGI_BIOE
Known GenesARID1A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997106
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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