A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023332



Internal ID19112549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63968448..64815193hg38UCSC Ensembl
Innerchr9:69178874..69827611hg19UCSC Ensembl
Innerchr9:68468694..69117431hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38846746
hg19648738
hg18648738
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7654n100
Supporting Variantsnssv3696079, nssv3696080
Samples
Known GenesANKRD20A4, CBWD5, CBWD6, FOXD4L6, LOC100133920, LOC440896
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023332
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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