A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv744078



Internal ID15691348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14595068..14624222hg38UCSC Ensembl
Innerchr10:14637067..14666221hg19UCSC Ensembl
Innerchr10:14677073..14706227hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3829155
hg1929155
hg1829155
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549998
Supporting Variants
Samples
Known GenesFAM107B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv744078
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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