A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027385



Internal ID18769917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:187992714..188017314hg38UCSC Ensembl
Innerchr4:188913868..188938468hg19UCSC Ensembl
Innerchr4:189150862..189175462hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3824601
hg1924601
hg1824601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636415
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)nsv1027385
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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