A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056064



Internal ID19145283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:2569035..2644461hg38UCSC Ensembl
Innerchr19:2569033..2644459hg19UCSC Ensembl
Innerchr19:2520033..2595459hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3875427
hg1975427
hg1875427
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3723251
Samples
Known GenesGNG7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056064
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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