A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv451152



Internal ID18621833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:85818044..86017244hg38UCSC Ensembl
Innerchr7:85447360..85646560hg19UCSC Ensembl
Innerchr7:85285296..85484496hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38199201
hg19199201
hg18199201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428176
Supporting Variants
SamplesNA19189
Known Genes
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)nssv451152
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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