A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042341



Internal ID19131560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30608663..30688830hg38UCSC Ensembl
Innerchr15:30900866..30981033hg19UCSC Ensembl
Innerchr15:28688158..28768325hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3880168
hg1980168
hg1880168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2528n100
Supporting Variantsnssv3547617, nssv3547619, nssv3721580, nssv3547616, nssv3547618
Samples
Known GenesARHGAP11B, GOLGA8H, LOC100288637
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042341
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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