A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043362



Internal ID18785893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58434138..58464372hg38UCSC Ensembl
Innerchr15:58726337..58756571hg19UCSC Ensembl
Innerchr15:56513629..56543863hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3830235
hg1930235
hg1830235
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553610
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)nsv1043362
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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