A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052724



Internal ID18795255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93026471..93079437hg38UCSC Ensembl
Innerchr15:93569701..93622666hg19UCSC Ensembl
Innerchr15:91370705..91423670hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3852967
hg1952966
hg1852966
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555233
Samples
Known GenesCHD2, RGMA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052724
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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