A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv831125



Internal ID6156849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:128412705..128595751hg19UCSC Ensembl
Outerchr7:128199941..128382987hg18UCSC Ensembl
Outerchr7:128006656..128189702hg17UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1446468, nssv1446467, nssv1446469
Samples
Known GenesATP6V1F, CALU, CCDC136, FLNC, IRF5, KCP, LOC100130705, OPN1SW, TNPO3
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv831125
Frequency
Sample Size95
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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