A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626800



Internal ID15503647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:666112..668145hg38UCSC Ensembl
Outerchr6:666112..668145hg19UCSC Ensembl
Outerchr6:611112..613145hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg382034
hg192034
hg182034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513290
Supporting Variants
Samples1
Known GenesEXOC2
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626800
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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