A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511252



Internal ID15503991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:6681178..6683527hg38UCSC Ensembl
Outerchr4:6678850..6685386hg38UCSC Ensembl
Innerchr4:6682905..6685254hg19UCSC Ensembl
Outerchr4:6680577..6687113hg19UCSC Ensembl
Innerchr4:6733806..6736155hg18UCSC Ensembl
Outerchr4:6731478..6738014hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg386537
hg196537
hg186537
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624699
Samples1
Known Genes
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511252
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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