A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997486



Internal ID16943752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:82389384..82395583hg38UCSC Ensembl
Outerchr6:83099101..83105300hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg386200
hg196200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950475
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997486
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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