A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965411



Internal ID18253959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:191346443..191353939hg38UCSC Ensembl
Innerchr3:191064232..191071728hg19UCSC Ensembl
Innerchr3:192546926..192554422hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg387497
hg197497
hg187497
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2762602, nssv2765626, nssv2758948
SamplesHGDP00998, HGDP00521, HGDP00927
Known GenesCCDC50
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965411
Frequency
Sample Size10
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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