A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027536



Internal ID19116755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63968448..64818927hg38UCSC Ensembl
Innerchr9:69186118..69831345hg19UCSC Ensembl
Innerchr9:68475938..69121165hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38850480
hg19645228
hg18645228
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7654n100
Supporting Variantsnssv3696096
Samples
Known GenesANKRD20A4, CBWD5, CBWD6, FOXD4L6, LOC100133920
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027536
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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