A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665564



Internal ID15402216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:122942790..122943908hg38UCSC Ensembl
Innerchr3:122661637..122662755hg19UCSC Ensembl
Innerchr3:124144327..124145445hg18UCSC Ensembl
Innerchr3:124144327..124145445hg17UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg381119
hg191119
hg181119
hg171119
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517695
Supporting Variants
Samples
Known GenesSEMA5B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665564
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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