A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv450918



Internal ID18619958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:6962388..7179922hg38UCSC Ensembl
Innerchr7:7002019..7219553hg19UCSC Ensembl
Innerchr7:6968544..7186078hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38217535
hg19217535
hg18217535
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428160
Supporting Variants
SamplesHGDP00462
Known GenesLOC100131257
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)nssv450918
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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