A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv752250



Internal ID16046206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86942593..86944294hg38UCSC Ensembl
Innerchr10:88702350..88704051hg19UCSC Ensembl
Innerchr10:88692330..88694031hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg381702
hg191702
hg181702
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551806
Supporting Variants
Samples
Known GenesMMRN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv752250
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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