A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025003



Internal ID18767535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:155077125..155755140hg38UCSC Ensembl
Innerchr6:155398259..156076274hg19UCSC Ensembl
Innerchr6:155439951..156117966hg18UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38678016
hg19678016
hg18678016
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654483
Samples
Known GenesCLDN20, NOX3, TFB1M, TIAM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025003
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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