A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020048



Internal ID19109267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:180499261..180546578hg38UCSC Ensembl
Innerchr4:181420414..181467731hg19UCSC Ensembl
Innerchr4:181657408..181704725hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3847318
hg1947318
hg1847318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3744529
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)nsv1020048
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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