A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035820



Internal ID18778351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30438488..30818328hg38UCSC Ensembl
Innerchr15:30730691..31110531hg19UCSC Ensembl
Innerchr15:28517983..28897823hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38379841
hg19379841
hg18379841
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2526n100
Supporting Variantsnssv3721571
Samples
Known GenesARHGAP11B, GOLGA8H, HERC2P10, 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)nsv1035820
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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