A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027029



Internal ID19116248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:74655132..74708251hg38UCSC Ensembl
Innerchr6:75364848..75417967hg19UCSC Ensembl
Innerchr6:75421568..75474687hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3853120
hg1953120
hg1853120
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6016n100
Supporting Variantsnssv3658816
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)nsv1027029
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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