A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061249



Internal ID18803780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14838727..14867472hg38UCSC Ensembl
Innerchr19:14949539..14978284hg19UCSC Ensembl
Innerchr19:14810539..14839284hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3828746
hg1928746
hg1828746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564779
Samples
Known GenesOR7A10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061249
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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