A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997536



Internal ID16943802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:154838667..154853166hg38UCSC Ensembl
Outerchr6:155159801..155174300hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3814500
hg1914500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv949870
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997536
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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