A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700207



Internal ID15090173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:78183449..78280693hg38UCSC Ensembl
Innerchr17:76179530..76276774hg19UCSC Ensembl
Innerchr17:73691125..73788369hg18UCSC Ensembl
Innerchr17:73691125..73788369hg17UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3897245
hg1997245
hg1897245
hg1797245
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524306
Supporting Variants
Samples
Known GenesAFMID, BIRC5, LOC100996291, TK1, TMEM235
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700207
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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