A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549984



Internal ID16337393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13014587..13018410hg38UCSC Ensembl
Innerchr10:13056587..13060410hg19UCSC Ensembl
Innerchr10:13096593..13100416hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg383824
hg193824
hg183824
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv959n54
Supporting Variantsnssv744043, nssv744045, nssv744041, nssv744044, nssv744042, nssv744036, nssv744057, nssv744056, nssv744039, nssv744048, nssv744040, nssv744053, nssv744047, nssv744055, nssv744058, nssv744051, nssv744054, nssv744046, nssv744050, nssv744037, nssv744038, nssv744052, nssv744049
Samples
Known GenesCCDC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549984
Frequency
Sample Size17421
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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