A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9389



Internal ID15540340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:21145448..21197639hg38UCSC Ensembl
Outerchr4:21147071..21199262hg19UCSC Ensembl
Outerchr4:20756169..20808360hg18UCSC Ensembl
Outerchr4:20823340..20875531hg17UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3852192
hg1952192
hg1852192
hg1752192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4264
Supporting Variants
SamplesNA18517
Known GenesKCNIP4
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)nssv9389
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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