A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048881



Internal ID18791412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30094196..30641319hg38UCSC Ensembl
Innerchr15:30386399..30933522hg19UCSC Ensembl
Innerchr15:28173691..28720814hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38547124
hg19547124
hg18547124
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2500n100
Supporting Variantsnssv3546462, nssv3546463
Samples
Known GenesARHGAP11B, CHRFAM7A, DKFZP434L187, GOLGA8H, 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)nsv1048881
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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