A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037817



Internal ID18780348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30350881..30608663hg38UCSC Ensembl
Innerchr15:30643084..30900866hg19UCSC Ensembl
Innerchr15:28430376..28688158hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38257783
hg19257783
hg18257783
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2520n100
Supporting Variantsnssv3546790, nssv3546789
Samples
Known GenesCHRFAM7A, GOLGA8H, LOC101059918, ULK4P1, ULK4P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037817
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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