A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035201



Internal ID18777732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30094196..30442542hg38UCSC Ensembl
Innerchr15:30386399..30734745hg19UCSC Ensembl
Innerchr15:28173691..28522037hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38348347
hg19348347
hg18348347
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2499n100
Supporting Variantsnssv3545694
Samples
Known GenesCHRFAM7A, DKFZP434L187, GOLGA8J, GOLGA8T, LOC101059918, ULK4P1, ULK4P2, ULK4P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035201
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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