A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001577



Internal ID19090794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:118525634..118568102hg38UCSC Ensembl
Innerchr1:119068257..119110725hg19UCSC Ensembl
Innerchr1:118869780..118912248hg18UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3842469
hg1942469
hg1842469
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3702059
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)nsv1001577
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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