A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3553631



Internal ID18851912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:61392006..61408173hg38UCSC Ensembl
Innerchr15:61684205..61700372hg19UCSC Ensembl
Innerchr15:59471497..59487664hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3816168
hg1916168
hg1816168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046354
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)nssv3553631
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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