A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024727



Internal ID19113944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:21739263..21853680hg38UCSC Ensembl
Innerchr8:21596775..21711191hg19UCSC Ensembl
Innerchr8:21641055..21767137hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38114418
hg19114417
hg18126083
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3685338
Samples
Known GenesGFRA2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024727
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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