A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv451668



Internal ID18273429
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 StatusS
Merged Variantsnsv428211
Supporting Variants
SamplesHGDP00467
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)nssv451668
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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