A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3638096



Internal ID18936377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8704114..8749652hg38UCSC Ensembl
Innerchr5:8704226..8749764hg19UCSC Ensembl
Innerchr5:8757226..8802764hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3845539
hg1945539
hg1845539
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032657
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)nssv3638096
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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