A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054763



Internal ID18797294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30608663..30687726hg38UCSC Ensembl
Innerchr15:30900866..30979929hg19UCSC Ensembl
Innerchr15:28688158..28767221hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3879064
hg1979064
hg1879064
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2528n100
Supporting Variantsnssv3547614, nssv3547615
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)nsv1054763
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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