A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001156



Internal ID19090373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34759898..34795691hg38UCSC Ensembl
Innerchr4:34761520..34797313hg19UCSC Ensembl
Innerchr4:34437915..34473708hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3835794
hg1935794
hg1835794
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5166n100
Supporting Variantsnssv3620656
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)nsv1001156
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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