A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3641181



Internal ID18939462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:139057974..139068387hg38UCSC Ensembl
Innerchr4:139979128..139989541hg19UCSC Ensembl
Innerchr4:140198578..140208991hg18UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3810414
hg1910414
hg1810414
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020743
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)nssv3641181
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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