A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035200



Internal ID19124419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20199589..21018342hg38UCSC Ensembl
Innerchr15:20404842..21223671hg19UCSC Ensembl
Innerchr15:18664856..19488330hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38818754
hg19818830
hg18823475
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2212n100
Supporting Variantsnssv3538160
Samples
Known GenesCHEK2P2, CT60, 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)nsv1035200
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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