A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008963



Internal ID19098181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:106361499..106463767hg38UCSC Ensembl
Innerchr4:107282656..107384924hg19UCSC Ensembl
Innerchr4:107502105..107604373hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38102269
hg19102269
hg18102269
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3632413
Samples
Known GenesGIMD1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008963
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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