A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968029



Internal ID18603257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152067789..152073304hg38UCSC Ensembl
Innerchr4:152988941..152994456hg19UCSC Ensembl
Innerchr4:153208391..153213906hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg385516
hg195516
hg185516
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2763929
SamplesHGDP01284
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968029
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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