A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040287



Internal ID18782818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30438488..30688830hg38UCSC Ensembl
Innerchr15:30730691..30981033hg19UCSC Ensembl
Innerchr15:28517983..28768325hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38250343
hg19250343
hg18250343
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2525n100
Supporting Variantsnssv3547584, nssv3547589, nssv3547587, nssv3547586, nssv3721569, nssv3547585, nssv3547588, nssv3721570
Samples
Known GenesARHGAP11B, GOLGA8H, LOC100288637, 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)nsv1040287
Frequency
Sample Size29084
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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