A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1048587



Internal ID15555087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:1610649..1623755hg38UCSC Ensembl
Innerchr6:1610884..1623990hg19UCSC Ensembl
Innerchr6:1555883..1568989hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3813107
hg1913107
hg1813107
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600807
Supporting Variants
Samples
Known GenesFOXC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1048587
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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