A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026136



Internal ID18768668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:88589781..88940524hg38UCSC Ensembl
Innerchr6:89299500..89650243hg19UCSC Ensembl
Innerchr6:89356219..89706962hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38350744
hg19350744
hg18350744
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6087n100
Supporting Variantsnssv3648947
Samples
Known GenesRNGTT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026136
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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