A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001493



Internal ID19090710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:185439824..185467710hg38UCSC Ensembl
Innerchr1:185408956..185436842hg19UCSC Ensembl
Innerchr1:183675579..183703465hg18UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3827887
hg1927887
hg1827887
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3704834
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)nsv1001493
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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