A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004167



Internal ID19093384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34763973..34823091hg38UCSC Ensembl
Innerchr4:34765595..34824713hg19UCSC Ensembl
Innerchr4:34441990..34501108hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3859119
hg1959119
hg1859119
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5167n100
Supporting Variantsnssv3620684, nssv3620685
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)nsv1004167
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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