A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052585



Internal ID18795116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84153209..84509904hg38UCSC Ensembl
Innerchr15:84821961..85053135hg19UCSC Ensembl
Innerchr15:82612965..82854139hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38356696
hg19231175
hg18241175
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2642n100
Supporting Variantsnssv3554639, nssv3554640
Samples
Known GenesDNM1P41, GOLGA6L4, GOLGA6L5P, LOC100505679, LOC388152, LOC440300, LOC642423
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052585
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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