A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3641183



Internal ID18592778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:139302827..139343882hg38UCSC Ensembl
Innerchr4:140223981..140265036hg19UCSC Ensembl
Innerchr4:140443431..140484486hg18UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3841056
hg1941056
hg1841056
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034429
Supporting Variants
Samples
Known GenesNAA15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3641183
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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