A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021951



Internal ID19111169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:95435005..95450433hg38UCSC Ensembl
Innerchr8:96447233..96462661hg19UCSC Ensembl
Innerchr8:96516409..96531837hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3815429
hg1915429
hg1815429
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7274n100
Supporting Variantsnssv3689734
Samples
Known GenesLOC100616530
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021951
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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