A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027585



Internal ID19116804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:124615683..124695497hg38UCSC Ensembl
Innerchr8:125627924..125707738hg19UCSC Ensembl
Innerchr8:125697105..125776919hg18UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3879815
hg1979815
hg1879815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691507
Samples
Known GenesMTSS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027585
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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