A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3556



Internal ID15538284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:97757809..97786191hg38UCSC Ensembl
Outerchr7:97387121..97415503hg19UCSC Ensembl
Outerchr7:97225057..97253439hg18UCSC Ensembl
Outerchr7:97031772..97060154hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3828383
hg1928383
hg1828383
hg1728383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858
Supporting Variants
SamplesNA12878
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)nssv3556
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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