A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003408



Internal ID19092626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:37167223..37214376hg38UCSC Ensembl
Innerchr1:37632824..37679977hg19UCSC Ensembl
Innerchr1:37405411..37452564hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3847154
hg1947154
hg1847154
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv150n100
Supporting Variantsnssv3466160
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003408
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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