A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3642129



Internal ID18940410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:53311906..53341292hg38UCSC Ensembl
Innerchr5:52607736..52637122hg19UCSC Ensembl
Innerchr5:52643493..52672879hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3829387
hg1929387
hg1829387
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020388
Supporting Variants
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)nssv3642129
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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