A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003402



Internal ID18745933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:144963817..145023143hg38UCSC Ensembl
Innerchr1:143982530..144045290hg19UCSC Ensembl
Innerchr1:142693888..142756647hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg3859327
hg1962761
hg1862760
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3486161
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)nsv1003402
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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