A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046354



Internal ID19135573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:61392006..61408173hg38UCSC Ensembl
Innerchr15:61684205..61700372hg19UCSC Ensembl
Innerchr15:59471497..59487664hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3816168
hg1916168
hg1816168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2614n100
Supporting Variantsnssv3553631
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)nsv1046354
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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