A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031778



Internal ID19121000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:163060696..163141573hg38UCSC Ensembl
Innerchr5:162487702..162568579hg19UCSC Ensembl
Innerchr5:162420280..162501157hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3880878
hg1980878
hg1880878
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648234
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)nsv1031778
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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