A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6981



Internal ID15536883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:34857316..34903338hg38UCSC Ensembl
Outerchr22:35253306..35299329hg19UCSC Ensembl
Outerchr22:33583306..33629329hg18UCSC Ensembl
Outerchr22:33577860..33623883hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3846023
hg1946024
hg1846024
hg1746024
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3607
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)nssv6981
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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