A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv752247



Internal ID16046203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86942575..86942967hg38UCSC Ensembl
Innerchr10:88702332..88702724hg19UCSC Ensembl
Innerchr10:88692312..88692704hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38393
hg19393
hg18393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551803
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)nssv752247
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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