A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703260



Internal ID15439912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:13610335..13611900hg38UCSC Ensembl
Innerchr3:13651835..13653400hg19UCSC Ensembl
Innerchr3:13626836..13628401hg18UCSC Ensembl
Innerchr3:13626836..13628401hg17UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg381566
hg191566
hg181566
hg171566
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526900
Supporting Variants
Samples
Known GenesFBLN2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703260
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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