A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7078



Internal ID15536786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:43728469..43773896hg38UCSC Ensembl
Outerchr4:43730486..43775913hg19UCSC Ensembl
Outerchr4:43425243..43470670hg18UCSC Ensembl
Outerchr4:43571414..43616841hg17UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3845428
hg1945428
hg1845428
hg1745428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4313
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)nssv7078
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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