A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035202



Internal ID19124421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32166460..32329014hg38UCSC Ensembl
Innerchr15:32458661..32621215hg19UCSC Ensembl
Innerchr15:30245953..30408507hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38162555
hg19162555
hg18162555
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3547728, nssv3547726, nssv3547727
Samples
Known GenesCHRNA7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035202
Frequency
Sample Size11257
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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