A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997988



Internal ID19157525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:121413177..121491079hg38UCSC Ensembl
Innerchr4:122334332..122412234hg19UCSC Ensembl
Innerchr4:122553782..122631684hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3877903
hg1977903
hg1877903
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5379n100
Supporting Variantsnssv3639387, nssv3639388, nssv3639390, nssv3639391, nssv3639386, nssv3639389, nssv3639392
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)nsv997988
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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