A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670750



Internal ID15060716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161721643..161730441hg38UCSC Ensembl
Innerchr1:161691433..161700231hg19UCSC Ensembl
Innerchr1:159958057..159966855hg18UCSC Ensembl
Innerchr1:158423091..158431889hg17UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg388799
hg198799
hg188799
hg178799
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516773
Supporting Variants
Samples
Known GenesFCRLB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670750
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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