A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701770



Internal ID15438422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6209289..6239252hg38UCSC Ensembl
Innerchr10:6251252..6281215hg19UCSC Ensembl
Innerchr10:6291258..6321221hg18UCSC Ensembl
Innerchr10:6291258..6321221hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3829964
hg1929964
hg1829964
hg1729964
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525622
Supporting Variants
Samples
Known GenesPFKFB3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701770
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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