A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004500



Internal ID19093718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:140302752..140470306hg38UCSC Ensembl
Innerchr3:140021594..140189148hg19UCSC Ensembl
Innerchr3:141504284..141671838hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38167555
hg19167555
hg18167555
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4910n100
Supporting Variantsnssv3606098
Samples
Known GenesCLSTN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004500
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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