A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035012



Internal ID19124231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:147642984..147676686hg38UCSC Ensembl
Innerchr6:147964120..147997822hg19UCSC Ensembl
Innerchr6:148005813..148039515hg18UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3833703
hg1933703
hg1833703
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749559
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)nsv1035012
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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