A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704556



Internal ID15094522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13988319..14253302hg38UCSC Ensembl
Innerchr10:14030319..14295301hg19UCSC Ensembl
Innerchr10:14070325..14335307hg18UCSC Ensembl
Innerchr10:14070325..14335307hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38264984
hg19264983
hg18264983
hg17264983
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528027
Supporting Variants
Samples
Known GenesFRMD4A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704556
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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