A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691507



Internal ID18989788
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 StatusS
Merged Variantsnsv1027585
Supporting Variants
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)nssv3691507
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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