A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4629



Internal ID15549357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:183151064..183195988hg38UCSC Ensembl
Outerchr4:184072217..184117141hg19UCSC Ensembl
Outerchr4:184309211..184354135hg18UCSC Ensembl
Outerchr4:184447366..184492290hg17UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3844925
hg1944925
hg1844925
hg1744925
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8040
SamplesNA12156
Known GenesWWC2
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)nsv4629
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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