A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034696



Internal ID19123917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:125280878..125319078hg38UCSC Ensembl
Innerchr5:124616571..124654771hg19UCSC Ensembl
Innerchr5:124644470..124682670hg18UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3838201
hg1938201
hg1838201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648093
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)nsv1034696
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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