A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000128



Internal ID19089345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37933317..37945304hg38UCSC Ensembl
Innerchr3:37974808..37986795hg19UCSC Ensembl
Innerchr3:37949812..37961799hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3811988
hg1911988
hg1811988
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4721n100
Supporting Variantsnssv3589676, nssv3589677
Samples
Known GenesCTDSPL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1000128
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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