A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149593



Internal ID15853820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:46801652..46852188hg38UCSC Ensembl
Innerchr15:47093850..47144386hg19UCSC Ensembl
Innerchr15:44881142..44931678hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3850537
hg1950537
hg1850537
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569322
Supporting Variants
Samples1780854449_A
Known GenesMIR548A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149593
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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