A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3641182



Internal ID18939463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:139100120..139122287hg38UCSC Ensembl
Innerchr4:140021274..140043441hg19UCSC Ensembl
Innerchr4:140240724..140262891hg18UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3822168
hg1922168
hg1822168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028153
Supporting Variants
Samples
Known GenesELF2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3641182
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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