A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6131



Internal ID15537732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:56683754..56712782hg38UCSC Ensembl
Outerchr7:56751447..56780475hg19UCSC Ensembl
Outerchr7:56718941..56747969hg18UCSC Ensembl
Outerchr7:56525656..56554684hg17UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3829029
hg1929029
hg1829029
hg1729029
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5759
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)nssv6131
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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