A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv752258



Internal ID16046214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86942633..86944294hg38UCSC Ensembl
Innerchr10:88702390..88704051hg19UCSC Ensembl
Innerchr10:88692370..88694031hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg381662
hg191662
hg181662
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551810
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)nssv752258
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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