A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021444



Internal ID19110661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:6374605..6392173hg38UCSC Ensembl
Innerchr8:6232126..6249694hg19UCSC Ensembl
Innerchr8:6219534..6237102hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3817569
hg1917569
hg1817569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6875n100
Supporting Variantsnssv3677424
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)nsv1021444
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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