A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174125



Internal ID15855013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13511345..13563368hg38UCSC Ensembl
Innerchr10:13553345..13605368hg19UCSC Ensembl
Innerchr10:13593351..13645374hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3852024
hg1952024
hg1852024
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549988
Supporting Variants
Samples1780862415_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174125
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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