A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614888



Internal ID16402297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:93708191..93720858hg38UCSC Ensembl
Innerchr9:96470473..96483140hg19UCSC Ensembl
Innerchr9:95510294..95522961hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3812668
hg1912668
hg1812668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12797n54
Supporting Variantsnssv1139497
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614888
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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