A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015931



Internal ID19105149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:185762011..185813326hg38UCSC Ensembl
Innerchr4:186683165..186734480hg19UCSC Ensembl
Innerchr4:186920159..186971474hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3851316
hg1951316
hg1851316
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635626
Samples
Known GenesSORBS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015931
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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