A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635564



Internal ID18933845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:179401776..179427294hg38UCSC Ensembl
Innerchr4:180322930..180348448hg19UCSC Ensembl
Innerchr4:180559924..180585442hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3825519
hg1925519
hg1825519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033718
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3635564
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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