A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040852



Internal ID18783383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76867896..77845199hg38UCSC Ensembl
Innerchr15:77160237..78137541hg19UCSC Ensembl
Innerchr15:74947292..75924596hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38977304
hg19977305
hg18977305
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3554582
Samples
Known GenesHMG20A, LINC00597, LINGO1, LOC253044, PEAK1, PSTPIP1, RCN2, SCAPER, TSPAN3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040852
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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