A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614205



Internal ID16401614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:36487197..36488264hg38UCSC Ensembl
Innerchr9:36487194..36488261hg19UCSC Ensembl
Innerchr9:36477194..36478261hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg381068
hg191068
hg181068
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12671n54
Supporting Variantsnssv1133961, nssv1133960
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614205
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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