A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044320



Internal ID18786851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:50724167..50781864hg38UCSC Ensembl
Innerchr15:51016364..51074061hg19UCSC Ensembl
Innerchr15:48803656..48861353hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3857698
hg1957698
hg1857698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552397
Samples
Known GenesSPPL2A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044320
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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