A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001453



Internal ID19090670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:165091699..165128580hg38UCSC Ensembl
Innerchr1:165060936..165097817hg19UCSC Ensembl
Innerchr1:163327560..163364441hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3836882
hg1936882
hg1836882
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3485777
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)nsv1001453
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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