A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057788



Internal ID19147007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15497917..15594886hg38UCSC Ensembl
Innerchr19:15608728..15705697hg19UCSC Ensembl
Innerchr19:15469728..15566697hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3896970
hg1996970
hg1896970
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564793
Samples
Known GenesCYP4F22
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057788
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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