A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019027



Internal ID19108244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12619983..12720569hg38UCSC Ensembl
Innerchr8:12477492..12578078hg19UCSC Ensembl
Innerchr8:12521863..12622449hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38100587
hg19100587
hg18100587
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7082n100
Supporting Variantsnssv3666975
Samples
Known GenesLOC729732
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019027
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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