A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042261



Internal ID19131480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:61395970..61408370hg38UCSC Ensembl
Innerchr15:61688169..61700569hg19UCSC Ensembl
Innerchr15:59475461..59487861hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3812401
hg1912401
hg1812401
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2614n100
Supporting Variantsnssv3553633, nssv3553632
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)nsv1042261
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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