A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051662



Internal ID19140881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:38363360..38396589hg38UCSC Ensembl
Innerchr15:38655561..38688790hg19UCSC Ensembl
Innerchr15:36442853..36476082hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3833230
hg1933230
hg1833230
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3716700
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)nsv1051662
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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