A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868



Internal ID15550720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:100572375..100617023hg38UCSC Ensembl
Outerchr7:100169998..100214646hg19UCSC Ensembl
Outerchr7:100007934..100052582hg18UCSC Ensembl
Outerchr7:99814649..99859297hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3844649
hg1944649
hg1844649
hg1744649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8406
SamplesNA12156
Known GenesFBXO24, LRCH4, MOSPD3, PCOLCE, PCOLCE-AS1, SAP25
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)nsv5868
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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