A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3555279



Internal ID18853560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:94238675..94285021hg38UCSC Ensembl
Innerchr15:94781904..94828250hg19UCSC Ensembl
Innerchr15:92582908..92629254hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3846347
hg1946347
hg1846347
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042975
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3555279
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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