A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003738



Internal ID19092956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:107280924..107296783hg38UCSC Ensembl
Innerchr4:108202081..108217940hg19UCSC Ensembl
Innerchr4:108421530..108437389hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3815860
hg1915860
hg1815860
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3632594, nssv3632595, nssv3632593, nssv3632592
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)nsv1003738
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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