A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595650



Internal ID16036373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:146125920..146222420hg38UCSC Ensembl
Innerchr4:147047072..147143572hg19UCSC Ensembl
Innerchr4:147266522..147363022hg18UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg3896501
hg1996501
hg1896501
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152839
Samples1798860336_A
Known GenesLSM6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595650
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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