A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015234



Internal ID19104451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:11545349..11583283hg38UCSC Ensembl
Innerchr6:11545582..11583516hg19UCSC Ensembl
Innerchr6:11653568..11691502hg18UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg3837935
hg1937935
hg1837935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654787
Samples
Known GenesTMEM170B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015234
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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