A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3648230



Internal ID18946511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:162184653..162212378hg38UCSC Ensembl
Innerchr5:161611659..161639384hg19UCSC Ensembl
Innerchr5:161544237..161571962hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3827726
hg1927726
hg1827726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018896
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)nssv3648230
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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