A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028897



Internal ID19118116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:46810668..46890345hg38UCSC Ensembl
Innerchr8:47722290..47801967hg19UCSC Ensembl
Innerchr8:47841455..47921132hg18UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg3879678
hg1979678
hg1879678
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3687451
Samples
Known GenesLINC00293
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028897
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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