A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4628



Internal ID15549356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:182990158..183028226hg38UCSC Ensembl
Outerchr4:183911311..183949379hg19UCSC Ensembl
Outerchr4:184148305..184186373hg18UCSC Ensembl
Outerchr4:184286460..184324528hg17UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3838069
hg1938069
hg1838069
hg1738069
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8039
SamplesNA12156
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv4628
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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