A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626



Internal ID15550454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:4788037..4819657hg38UCSC Ensembl
Outerchr7:4827668..4859288hg19UCSC Ensembl
Outerchr7:4794194..4825814hg18UCSC Ensembl
Outerchr7:4600909..4632529hg17UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg387882
hg197882
hg187882
hg177882
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10532
SamplesNA18956
Known GenesAP5Z1, MIR4656, RADIL
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv5626
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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