A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039778



Internal ID18782309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30638297..30688830hg38UCSC Ensembl
Innerchr15:30930500..30981033hg19UCSC Ensembl
Innerchr15:28717792..28768325hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3850534
hg1950534
hg1850534
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2531n100
Supporting Variantsnssv3547644, nssv3547645, nssv3547643
Samples
Known GenesARHGAP11B, LOC100288637
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039778
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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