A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041172



Internal ID18783703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100435008..101062634hg38UCSC Ensembl
Innerchr15:100975213..101602839hg19UCSC Ensembl
Innerchr15:98792736..99420362hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38627627
hg19627627
hg18627627
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555329
Samples
Known GenesALDH1A3, ASB7, CERS3, LINS, LRRK1, PRKXP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041172
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer