A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv756252



Internal ID16050208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105865495..105939468hg38UCSC Ensembl
Innerchr10:107625253..107699226hg19UCSC Ensembl
Innerchr10:107615243..107689216hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3873974
hg1973974
hg1873974
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552102
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv756252
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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