A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968028



Internal ID18603256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:151869249..151874413hg38UCSC Ensembl
Innerchr4:152790401..152795565hg19UCSC Ensembl
Innerchr4:153009851..153015015hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg385165
hg195165
hg185165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2764371, nssv2756717
SamplesHGDP00665, HGDP00998
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968028
Frequency
Sample Size10
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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