A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021378



Internal ID18763912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:188381493..189834486hg38UCSC Ensembl
Innerchr4:189302647..190755641hg19UCSC Ensembl
Innerchr4:189539641..190992635hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg381452994
hg191452995
hg181452995
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3744546
Samples
Known GenesLINC01060
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021378
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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