A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516198



Internal ID15096805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13007885..13018410hg38UCSC Ensembl
Innerchr10:13049885..13060410hg19UCSC Ensembl
Innerchr10:13089891..13100416hg18UCSC Ensembl
Innerchr10:13089891..13100416hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3810526
hg1910526
hg1810526
hg1710526
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv672959, nssv677256, nssv683270, nssv681400, nssv693991, nssv662647, nssv662676, nssv668696, nssv655165, nssv661648, nssv657911, nssv662373, nssv692047, nssv700716, nssv690251, nssv659680, nssv666741, nssv687541, nssv681497, nssv683490, nssv661705, nssv659364, nssv668378, nssv656194, nssv672127, nssv684063
Samples
Known GenesCCDC3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516198
Frequency
Sample Size2026
Observed Gain0
Observed Loss26
Observed Complex0
Frequencyn/a


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