A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615418



Internal ID16402827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129176634..129204660hg38UCSC Ensembl
Innerchr9:131938913..131966939hg19UCSC Ensembl
Innerchr9:130978734..131006760hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3828027
hg1928027
hg1828027
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176006
Samples1780862304_A
Known GenesIER5L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615418
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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