A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028255



Internal ID19117473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136676662..136851683hg38UCSC Ensembl
Innerchr8:137688905..137863926hg19UCSC Ensembl
Innerchr8:137758087..137933108hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38175022
hg19175022
hg18175022
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7325n100
Supporting Variantsnssv3690039, nssv3690040
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028255
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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