A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053781



Internal ID18796312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136590694..136722927hg38UCSC Ensembl
Innerchr9:139485146..139617379hg19UCSC Ensembl
Innerchr9:138604967..138737200hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38132234
hg19132234
hg18132234
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3696510
Samples
Known GenesAGPAT2, EGFL7, FAM69B, MIR126
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053781
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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