A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058277



Internal ID18800808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:50985288..51006591hg38UCSC Ensembl
Innerchr19:51488544..51509847hg19UCSC Ensembl
Innerchr19:56180356..56201659hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3821304
hg1921304
hg1821304
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3574996
Samples
Known GenesKLK8, KLK9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058277
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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