A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053277



Internal ID18795808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30077711..30795118hg38UCSC Ensembl
Innerchr15:30369914..31087321hg19UCSC Ensembl
Innerchr15:28157206..28874613hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38717408
hg19717408
hg18717408
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2496n100
Supporting Variantsnssv3545681
Samples
Known GenesARHGAP11B, CHRFAM7A, DKFZP434L187, GOLGA8H, GOLGA8J, GOLGA8T, LOC100288637, 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)nsv1053277
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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