A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037061



Internal ID19126280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43600874..43698218hg38UCSC Ensembl
Innerchr15:43893072..43990416hg19UCSC Ensembl
Innerchr15:41680364..41777708hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3897345
hg1997345
hg1897345
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2585n100
Supporting Variantsnssv3552316
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)nsv1037061
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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