A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694891



Internal ID15084857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:108756961..109199392hg38UCSC Ensembl
Innerchr3:108475808..108918239hg19UCSC Ensembl
Innerchr3:109958498..110400929hg18UCSC Ensembl
Innerchr3:109958498..110400929hg17UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38442432
hg19442432
hg18442432
hg17442432
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522119
Supporting Variants
Samples
Known GenesFLJ22763, GUCA1C, LINC00488, MORC1, RETNLB, TRAT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694891
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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