A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043273



Internal ID18785804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:50712487..50751560hg38UCSC Ensembl
Innerchr15:51004684..51043757hg19UCSC Ensembl
Innerchr15:48791976..48831049hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3839074
hg1939074
hg1839074
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552396
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)nsv1043273
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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