A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3657434



Internal ID18609029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:44910316..45283714hg38UCSC Ensembl
Innerchr6:44878053..45251451hg19UCSC Ensembl
Innerchr6:44986031..45359429hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38373399
hg19373399
hg18373399
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024370
Supporting Variants
Samples
Known GenesMIR586, SUPT3H
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3657434
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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