A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004725



Internal ID19093942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:38462872..38532347hg38UCSC Ensembl
Innerchr4:38464493..38533968hg19UCSC Ensembl
Innerchr4:38140888..38210363hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3869476
hg1969476
hg1869476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5192n100
Supporting Variantsnssv3739352
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)nsv1004725
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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