A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000555



Internal ID19089772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:7798131..7943328hg38UCSC Ensembl
Innerchr3:7839818..7985015hg19UCSC Ensembl
Innerchr3:7814818..7960015hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38145198
hg19145198
hg18145198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4676n100
Supporting Variantsnssv3591837
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)nsv1000555
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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