A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044912



Internal ID18787443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30376250..30688830hg38UCSC Ensembl
Innerchr15:30668453..30981033hg19UCSC Ensembl
Innerchr15:28455745..28768325hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38312581
hg19312581
hg18312581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2517n100
Supporting Variantsnssv3547573
Samples
Known GenesARHGAP11B, CHRFAM7A, 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)nsv1044912
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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