A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511353



Internal ID15850778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:88091498..88092576hg38UCSC Ensembl
Outerchr6:88087979..88093881hg38UCSC Ensembl
Innerchr6:88801216..88802294hg19UCSC Ensembl
Outerchr6:88797697..88803599hg19UCSC Ensembl
Innerchr6:88857935..88859013hg18UCSC Ensembl
Outerchr6:88854416..88860318hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg385903
hg195903
hg185903
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625822
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)nsv511353
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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