A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038367



Internal ID19127586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:71516688..71574375hg38UCSC Ensembl
Innerchr9:74131604..74189291hg19UCSC Ensembl
Innerchr9:73321424..73379111hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3857688
hg1957688
hg1857688
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7677n100
Supporting Variantsnssv3696354
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038367
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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