A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615



Internal ID15203756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:1528557..1573208hg38UCSC Ensembl
Outerchr7:1568193..1612844hg19UCSC Ensembl
Outerchr7:1534719..1579370hg18UCSC Ensembl
Outerchr7:1341434..1386085hg17UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3844652
hg1944652
hg1844652
hg1744652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8334
SamplesNA12156
Known GenesMAFK, PSMG3, PSMG3-AS1, TMEM184A
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)nsv5615
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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