A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026918



Internal ID19116136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:10502124..10532942hg38UCSC Ensembl
Innerchr8:10359634..10390452hg19UCSC Ensembl
Innerchr8:10397044..10427862hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3830819
hg1930819
hg1830819
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3681720
Samples
Known GenesPRSS55
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026918
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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