A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv758788



Internal ID16052744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:115469284..115561010hg38UCSC Ensembl
Innerchr10:117228794..117320520hg19UCSC Ensembl
Innerchr10:117218784..117310510hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3891727
hg1991727
hg1891727
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552206
Supporting Variants
Samples
Known GenesATRNL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv758788
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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