A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7077



Internal ID15536787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:42809795..42829013hg38UCSC Ensembl
Outerchr4:42811812..42831030hg19UCSC Ensembl
Outerchr4:42506569..42525787hg18UCSC Ensembl
Outerchr4:42652740..42671958hg17UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3819219
hg1919219
hg1819219
hg1719219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4312
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)nssv7077
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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