A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020401



Internal ID19109620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63968448..64683570hg38UCSC Ensembl
Innerchr9:69178874..69695988hg19UCSC Ensembl
Innerchr9:68468694..68985808hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38715123
hg19517115
hg18517115
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7653n100
Supporting Variantsnssv3696078
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)nsv1020401
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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