A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv452849



Internal ID18274784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101192611..101376281hg38UCSC Ensembl
Innerchr15:101732816..101916486hg19UCSC Ensembl
Innerchr15:99550339..99734009hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38183671
hg19183671
hg18183671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428314
Supporting Variants
SamplesNA19108
Known GenesCHSY1, LOC100507472, PCSK6, SNRPA1, VIMP
MethodBAC aCGH
AnalysisCopy number variable segments were automatically detected using the CNVfinder algorithm (Fiegler et al. 2006).
PlatformSanger H. sapiens Whole Genome Tile Path 28.7k v3
Comments
ReferencePerry_et_al_2008b
Pubmed ID18775914
Accession Number(s)nssv452849
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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