A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4357



Internal ID15549058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:61087707..61094952hg38UCSC Ensembl
Outerchr4:61953425..61960670hg19UCSC Ensembl
Outerchr4:61636020..61643265hg18UCSC Ensembl
Outerchr4:61782191..61789436hg17UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg387246
hg197246
hg187246
hg177246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7961
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)nsv4357
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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