A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2756717



Internal ID17831984
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 Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv968028
Supporting Variants
SamplesHGDP00998
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2756717
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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