A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595120



Internal ID16035843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:107897601..107966289hg38UCSC Ensembl
Innerchr4:108818757..108887445hg19UCSC Ensembl
Innerchr4:109038206..109106894hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3868689
hg1968689
hg1868689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153160
Samples1782681102_A
Known GenesCYP2U1, SGMS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595120
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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