A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041622



Internal ID18784153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30608663..30796262hg38UCSC Ensembl
Innerchr15:30900866..31088465hg19UCSC Ensembl
Innerchr15:28688158..28875757hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38187600
hg19187600
hg18187600
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2529n100
Supporting Variantsnssv3547624, nssv3547625, nssv3547626
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)nsv1041622
Frequency
Sample Size29084
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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