A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027719



Internal ID19116938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:86035482..86616593hg38UCSC Ensembl
Innerchr6:86745200..87326311hg19UCSC Ensembl
Innerchr6:86801919..87383030hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38581112
hg19581112
hg18581112
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6080n100
Supporting Variantsnssv3750119
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)nsv1027719
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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