A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027064



Internal ID19116283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:39016598..39066740hg38UCSC Ensembl
Innerchr6:38984374..39034516hg19UCSC Ensembl
Innerchr6:39092352..39142494hg18UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3850143
hg1950143
hg1850143
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657429
Samples
Known GenesDNAH8, GLP1R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027064
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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