A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003708



Internal ID19092926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:27506383..27571488hg38UCSC Ensembl
Innerchr4:27508005..27573110hg19UCSC Ensembl
Innerchr4:27117103..27182208hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3865106
hg1965106
hg1865106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3620616
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)nsv1003708
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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