A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997559



Internal ID16943825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:167316413..167330812hg38UCSC Ensembl
Outerchr6:167729901..167744300hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3814400
hg1914400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv949893
Supporting Variants
SamplesBILGI_BIOE
Known GenesTTLL2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997559
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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