A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1004180



Internal ID16298136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:107585427..107593454hg38UCSC Ensembl
Innerchr4:108506584..108514610hg19UCSC Ensembl
Innerchr4:108726033..108734059hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg388028
hg198027
hg188027
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595099
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1004180
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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