A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008744



Internal ID19097961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:116153244..117256993hg38UCSC Ensembl
Innerchr4:117074400..118178149hg19UCSC Ensembl
Innerchr4:117293849..118397597hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg381103750
hg191103750
hg181103749
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639333
Samples
Known GenesMIR1973, TRAM1L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008744
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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