A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603770



Internal ID16391179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:75490798..75567580hg38UCSC Ensembl
Innerchr6:76200514..76277296hg19UCSC Ensembl
Innerchr6:76257234..76334016hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3876783
hg1976783
hg1876783
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1064529
Samples
Known GenesFILIP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603770
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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