A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950769



Internal ID17299643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:11575668..11585367hg38UCSC Ensembl
Outerchr6:11575901..11585600hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg389700
hg199700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997400
SamplesBILGI_BIOE
Known GenesTMEM170B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950769
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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