A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000947



Internal ID19090164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:105729996..105780522hg38UCSC Ensembl
Innerchr4:106651153..106701679hg19UCSC Ensembl
Innerchr4:106870602..106921128hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3850527
hg1950527
hg1850527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3632410
Samples
Known GenesGSTCD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1000947
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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