A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428176



Internal ID18624626
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 StatusM
Merged Variants
Supporting Variantsnssv451150, nssv451151, nssv451152
SamplesNA19189, NA19181, NA19113
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)nsv428176
Frequency
Sample Size62
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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