A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4772



Internal ID15543182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:103003411..103034963hg38UCSC Ensembl
Outerchr4:103924568..103956120hg19UCSC Ensembl
Outerchr4:104144017..104175569hg18UCSC Ensembl
Outerchr4:104282172..104313724hg17UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg387720
hg197720
hg187720
hg177720
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4445
Supporting Variants
SamplesNA19129
Known GenesSLC9B1, SLC9B2
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)nssv4772
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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