A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002121



Internal ID19091338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:44967371..45004306hg38UCSC Ensembl
Innerchr4:44969388..45006323hg19UCSC Ensembl
Innerchr4:44664145..44701080hg18UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3836936
hg1936936
hg1836936
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5199n100
Supporting Variantsnssv3625122
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)nsv1002121
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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