A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001035



Internal ID19090252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37933317..37945425hg38UCSC Ensembl
Innerchr3:37974808..37986916hg19UCSC Ensembl
Innerchr3:37949812..37961920hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3812109
hg1912109
hg1812109
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4721n100
Supporting Variantsnssv3589678, nssv3739696, nssv3739697
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)nsv1001035
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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