A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049646



Internal ID19138865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126440294..126489614hg38UCSC Ensembl
Innerchr9:129202573..129251893hg19UCSC Ensembl
Innerchr9:128242394..128291714hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3849321
hg1949321
hg1849321
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695248
Samples
Known GenesMVB12B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049646
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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