A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036109



Internal ID18778640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30201146..30654454hg38UCSC Ensembl
Innerchr15:30493349..30946657hg19UCSC Ensembl
Innerchr15:28280641..28733949hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38453309
hg19453309
hg18453309
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2504n100
Supporting Variantsnssv3546620, nssv3546621
Samples
Known GenesARHGAP11B, CHRFAM7A, DKFZP434L187, GOLGA8H, LOC100288637, 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)nsv1036109
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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