A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614690



Internal ID16402099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:75561615..75638471hg38UCSC Ensembl
Innerchr9:78176531..78253387hg19UCSC Ensembl
Innerchr9:77366351..77443207hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3876857
hg1976857
hg1876857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1137505
Samples
Known GenesMIR548H3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614690
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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