A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047564



Internal ID18790095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:74116495..74165840hg38UCSC Ensembl
Innerchr15:74408836..74458181hg19UCSC Ensembl
Innerchr15:72195889..72245234hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3849346
hg1949346
hg1849346
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553696
Samples
Known GenesISLR2, LOC283731
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047564
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