A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151770



Internal ID15534245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:50140578..50287241hg38UCSC Ensembl
Innerchr3:50178011..50324672hg19UCSC Ensembl
Innerchr3:50153015..50299676hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38146664
hg19146662
hg18146662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590252
Supporting Variants
SamplesNINDS_49
Known GenesGNAI2, GNAT1, LSMEM2, MIR5787, MIR6872, SEMA3B, SEMA3F, SLC38A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151770
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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