A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv752242



Internal ID16046198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86942473..86943239hg38UCSC Ensembl
Innerchr10:88702230..88702996hg19UCSC Ensembl
Innerchr10:88692210..88692976hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38767
hg19767
hg18767
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551800
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)nssv752242
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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