A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613191



Internal ID16400600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5306824..5355536hg38UCSC Ensembl
Innerchr9:5306824..5355536hg19UCSC Ensembl
Innerchr9:5296824..5345536hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3848713
hg1948713
hg1848713
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156216
Samples1780846005_A
Known GenesRLN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613191
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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