A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5752



Internal ID15203907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:54995331..55040249hg38UCSC Ensembl
Outerchr7:55063024..55107942hg19UCSC Ensembl
Outerchr7:55030518..55075436hg18UCSC Ensembl
Outerchr7:54837233..54882151hg17UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3844919
hg1944919
hg1844919
hg1744919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8377
SamplesNA12156
Known GenesEGFR
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)nsv5752
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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