A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614862



Internal ID16402271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:91633777..91641031hg38UCSC Ensembl
Innerchr9:94396059..94403313hg19UCSC Ensembl
Innerchr9:93435880..93443134hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg387255
hg197255
hg187255
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12792n54
Supporting Variantsnssv1139331, nssv1139330, nssv1139337, nssv1139328, nssv1139329, nssv1139332, nssv1139333, nssv1139335, nssv1139334, nssv1139336
Samples
Known GenesMIR3910-1, MIR3910-2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614862
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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