A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949899



Internal ID17298773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:168355521..168397020hg38UCSC Ensembl
Outerchr6:168756201..168797700hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3841500
hg1941500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997565
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949899
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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