A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023586



Internal ID19112803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:57283937..57311522hg38UCSC Ensembl
Innerchr8:58196496..58224081hg19UCSC Ensembl
Innerchr8:58359050..58386635hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3827586
hg1927586
hg1827586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3688709
Samples
Known GenesLINC00588
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023586
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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