A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013517



Internal ID19102735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:19609444..19653693hg38UCSC Ensembl
Innerchr4:19611067..19655316hg19UCSC Ensembl
Innerchr4:19220165..19264414hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3844250
hg1944250
hg1844250
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3737709, nssv3737708, nssv3619877, nssv3619878, nssv3619876
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)nsv1013517
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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