A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020605



Internal ID19109824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38518509..38989369hg38UCSC Ensembl
Innerchr9:38518506..38989366hg19UCSC Ensembl
Innerchr9:38508506..38979366hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38470861
hg19470861
hg18470861
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3688891
Samples
Known GenesANKRD18A, FAM201A, FAM95C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020605
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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