A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000438



Internal ID19089655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:104481103..104718359hg38UCSC Ensembl
Innerchr3:104199947..104437203hg19UCSC Ensembl
Innerchr3:105682637..105919893hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38237257
hg19237257
hg18237257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3735243
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)nsv1000438
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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