A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036320



Internal ID19125539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:99029171..99127521hg38UCSC Ensembl
Innerchr15:99572400..99667726hg19UCSC Ensembl
Innerchr15:97389923..97485249hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3898351
hg1995327
hg1895327
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555291
Samples
Known GenesSYNM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036320
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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