A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549982



Internal ID16337391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13014587..13018148hg38UCSC Ensembl
Innerchr10:13056587..13060148hg19UCSC Ensembl
Innerchr10:13096593..13100154hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg383562
hg193562
hg183562
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv959n54
Supporting Variantsnssv744025, nssv744021, nssv744022, nssv744024, nssv744020, nssv744026, nssv744027, nssv744023, nssv744019
Samples
Known GenesCCDC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549982
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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