A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038831



Internal ID19128050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20359322..20404354hg38UCSC Ensembl
Innerchr15:20564575..20609607hg19UCSC Ensembl
Innerchr15:18824589..18869621hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3845033
hg1945033
hg1845033
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2260n100
Supporting Variantsnssv3536391, nssv3536394, nssv3536392, nssv3536396, nssv3536395, nssv3536393
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038831
Frequency
Sample Size11257
Observed Gain2
Observed Loss4
Observed Complex0
Frequencyn/a


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