A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039442



Internal ID19128661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135276268..135414504hg38UCSC Ensembl
Innerchr9:138168114..138306350hg19UCSC Ensembl
Innerchr9:137307935..137446171hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38138237
hg19138237
hg18138237
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7726n100
Supporting Variantsnssv3696500
Samples
Known GenesC9orf62
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039442
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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