A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3555200



Internal ID18853481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90283720..90313106hg38UCSC Ensembl
Innerchr15:90826952..90856338hg19UCSC Ensembl
Innerchr15:88627956..88657342hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3829387
hg1929387
hg1829387
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054724
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)nssv3555200
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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