A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694178



Internal ID15084144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14602768..14630122hg38UCSC Ensembl
Innerchr10:14644767..14672121hg19UCSC Ensembl
Innerchr10:14684773..14712127hg18UCSC Ensembl
Innerchr10:14684773..14712127hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3827355
hg1927355
hg1827355
hg1727355
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517896
Supporting Variants
Samples
Known GenesFAM107B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694178
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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