A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041625



Internal ID18784156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:134261330..134453280hg38UCSC Ensembl
Innerchr9:137153176..137345126hg19UCSC Ensembl
Innerchr9:136292997..136484947hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38191951
hg19191951
hg18191951
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7722n100
Supporting Variantsnssv3696415, nssv3696414, nssv3696416, nssv3696417
Samples
Known GenesMIR4669, RXRA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041625
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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