A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026621



Internal ID19115839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:2043999..2067934hg38UCSC Ensembl
Innerchr8:1992115..2016053hg19UCSC Ensembl
Innerchr8:1979522..2003460hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3823936
hg1923939
hg1823939
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6807n100
Supporting Variantsnssv3675071
Samples
Known GenesMYOM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026621
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer