A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4155



Internal ID15202150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:186850087..186899316hg38UCSC Ensembl
Outerchr3:186567876..186617105hg19UCSC Ensembl
Outerchr3:188050570..188099799hg18UCSC Ensembl
Outerchr3:188050578..188099807hg17UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3849230
hg1949230
hg1849230
hg1749230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv11071, nssv354, nssv2437, nssv7904, nssv4701, nssv3219
SamplesNA15510, NA19129, NA12156, NA12878, NA19240, NA18555
Known GenesADIPOQ, ADIPOQ-AS1
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)nsv4155
Frequency
Sample Size9
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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