A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028995



Internal ID19118214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149649..254283hg38UCSC Ensembl
Innerchr6:149649..254283hg19UCSC Ensembl
Innerchr6:94649..199283hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38104635
hg19104635
hg18104635
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5867n100
Supporting Variantsnssv3650368
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)nsv1028995
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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