A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004414



Internal ID19093632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34759898..34802678hg38UCSC Ensembl
Innerchr4:34761520..34804300hg19UCSC Ensembl
Innerchr4:34437915..34480695hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3842781
hg1942781
hg1842781
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5166n100
Supporting Variantsnssv3620658
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)nsv1004414
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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