A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625566



Internal ID15849099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:47597040..47598833hg38UCSC Ensembl
Outerchr6:47590249..47609233hg38UCSC Ensembl
Innerchr6:47564776..47566569hg19UCSC Ensembl
Outerchr6:47557985..47576969hg19UCSC Ensembl
Innerchr6:47672735..47674528hg18UCSC Ensembl
Outerchr6:47665944..47684928hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3818985
hg1918985
hg1818985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511330
Supporting Variants
Samples1
Known GenesCD2AP
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv625566
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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