A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005572



Internal ID19094789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:44964987..45015559hg38UCSC Ensembl
Innerchr4:44967004..45017576hg19UCSC Ensembl
Innerchr4:44661761..44712333hg18UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3850573
hg1950573
hg1850573
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5199n100
Supporting Variantsnssv3739395
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)nsv1005572
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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