A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4961



Internal ID15544084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:906830..908439hg38UCSC Ensembl
Outerchr7:946467..948076hg19UCSC Ensembl
Outerchr7:912993..914602hg18UCSC Ensembl
Outerchr7:719708..721317hg17UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3812281
hg1912281
hg1812281
hg1712281
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5611
Supporting Variants
SamplesNA19129
Known GenesADAP1
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)nssv4961
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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