A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010638



Internal ID19099855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:119665023..119750680hg38UCSC Ensembl
Innerchr4:120586178..120671835hg19UCSC Ensembl
Innerchr4:120805626..120891283hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3885658
hg1985658
hg1885658
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5374n100
Supporting Variantsnssv3639350
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)nsv1010638
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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