A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034631



Internal ID19123853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:144993779..145029411hg38UCSC Ensembl
Innerchr5:144373342..144408974hg19UCSC Ensembl
Innerchr5:144353535..144389167hg18UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3835633
hg1935633
hg1835633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5815n100
Supporting Variantsnssv3648154, nssv3648153
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)nsv1034631
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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