A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3747904



Internal ID19046185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:4255406..4471401hg38UCSC Ensembl
Innerchr6:4255640..4471635hg19UCSC Ensembl
Innerchr6:4200639..4416634hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38215996
hg19215996
hg18215996
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027498
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3747904
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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