A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428211



Internal ID18277975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38451653..38619162hg38UCSC Ensembl
Innerchr9:38451650..38619159hg19UCSC Ensembl
Innerchr9:38441650..38609159hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38167510
hg19167510
hg18167510
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv451668, nssv451667
SamplesHGDP00467, HGDP00449
Known GenesANKRD18A, FAM95C
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)nsv428211
Frequency
Sample Size62
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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