A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589416



Internal ID16030139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4046892..4059672hg38UCSC Ensembl
Innerchr3:4088576..4101356hg19UCSC Ensembl
Innerchr3:4063576..4076356hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3812781
hg1912781
hg1812781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8177n54
Supporting Variantsnssv958015, nssv958013, nssv1152448, nssv958010, nssv958012, nssv1152449, nssv1152451, nssv958014, nssv958011, nssv1152450
SamplesNINDS_115, HGDP01357, NINDS_223, NINDS_51
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589416
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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