A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043560



Internal ID19132779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58559170..58571327hg38UCSC Ensembl
Innerchr15:58851369..58863526hg19UCSC Ensembl
Innerchr15:56638661..56650818hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3812158
hg1912158
hg1812158
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2608n100
Supporting Variantsnssv3553613
Samples
Known GenesLIPC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043560
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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