A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997551



Internal ID16943817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:163414069..163415668hg38UCSC Ensembl
Outerchr6:163835101..163836700hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv949885
Supporting Variants
SamplesBILGI_BIOE
Known GenesQKI
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997551
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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