A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037105



Internal ID19126324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90283720..90318370hg38UCSC Ensembl
Innerchr15:90826952..90861602hg19UCSC Ensembl
Innerchr15:88627956..88662606hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3834651
hg1934651
hg1834651
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2657n100
Supporting Variantsnssv3555201
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)nsv1037105
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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