A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035008



Internal ID19124227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:131025220..131443017hg38UCSC Ensembl
Innerchr4:131946375..132364172hg19UCSC Ensembl
Innerchr4:132165825..132583622hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38417798
hg19417798
hg18417798
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5388n100
Supporting Variantsnssv3639473, nssv3639471, nssv3639472
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)nsv1035008
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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