A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029725



Internal ID19118944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:86081165..86653306hg38UCSC Ensembl
Innerchr6:86790883..87363024hg19UCSC Ensembl
Innerchr6:86847602..87419743hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38572142
hg19572142
hg18572142
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6080n100
Supporting Variantsnssv3648904
Samples
Known GenesMIR548AD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029725
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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