A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042634



Internal ID18785165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:131116646..131247825hg38UCSC Ensembl
Innerchr10:132914909..133046088hg19UCSC Ensembl
Innerchr10:132804899..132936078hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38131180
hg19131180
hg18131180
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3512408
Samples
Known GenesTCERG1L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042634
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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