A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039652



Internal ID18782183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:69204723..69258106hg38UCSC Ensembl
Innerchr15:69497062..69550445hg19UCSC Ensembl
Innerchr15:67284116..67337499hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3853384
hg1953384
hg1853384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553662
Samples
Known GenesGLCE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039652
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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