A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv832425



Internal ID6158149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:10903845..11122975hg19UCSC Ensembl
Outerchr1:10826432..11045562hg18UCSC Ensembl
Outerchr1:10838111..11057241hg17UCSC Ensembl
Cytoband1p36.22
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 Variantsnssv1442729, nssv1442741
Samples
Known GenesC1orf127, MASP2, SRM, TARDBP
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv832425
Frequency
Sample Size95
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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