A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035225



Internal ID19124444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20217113..20926480hg38UCSC Ensembl
Innerchr15:20422366..21131809hg19UCSC Ensembl
Innerchr15:18682380..19396468hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38709368
hg19709444
hg18714089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2211n100
Supporting Variantsnssv3539373
Samples
Known GenesCHEK2P2, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, POTEB, POTEB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035225
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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