A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058745



Internal ID19147964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:7218124..7241294hg38UCSC Ensembl
Innerchr19:7218135..7241305hg19UCSC Ensembl
Innerchr19:7169135..7192305hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3823171
hg1923171
hg1823171
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564670
Samples
Known GenesINSR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058745
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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