A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030775



Internal ID18773306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:187983480..188060286hg38UCSC Ensembl
Innerchr4:188904634..188981440hg19UCSC Ensembl
Innerchr4:189141628..189218434hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3876807
hg1976807
hg1876807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636414
Samples
Known GenesZFP42
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030775
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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