A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036941



Internal ID19126160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43600874..43696114hg38UCSC Ensembl
Innerchr15:43893072..43988312hg19UCSC Ensembl
Innerchr15:41680364..41775604hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3895241
hg1995241
hg1895241
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2585n100
Supporting Variantsnssv3552306, nssv3552307
Samples
Known GenesCATSPER2, CKMT1A, RNU6-28P, STRC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036941
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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