A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8380



Internal ID15535484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:56592390..56637640hg38UCSC Ensembl
Outerchr7:56660083..56705333hg19UCSC Ensembl
Outerchr7:56627577..56672827hg18UCSC Ensembl
Outerchr7:56434292..56479542hg17UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3845251
hg1945251
hg1845251
hg1745251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5758
Supporting Variants
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)nssv8380
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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