A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997434



Internal ID16943700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:36029224..36041723hg38UCSC Ensembl
Outerchr6:35997001..36009500hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3812500
hg1912500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950162
Supporting Variants
SamplesBILGI_BIOE
Known GenesMAPK14
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997434
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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