A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591303



Internal ID16378712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:113841173..113890556hg38UCSC Ensembl
Innerchr3:113560020..113609403hg19UCSC Ensembl
Innerchr3:115042710..115092093hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3849384
hg1949384
hg1849384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8506n54
Supporting Variantsnssv971534
Samples
Known GenesGRAMD1C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591303
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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