A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6118



Internal ID15537745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:22978400..23023846hg38UCSC Ensembl
Outerchr7:23018019..23063465hg19UCSC Ensembl
Outerchr7:22984544..23029990hg18UCSC Ensembl
Outerchr7:22791259..22836705hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3845447
hg1945447
hg1845447
hg1745447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5660
Supporting Variants
SamplesNA12156
Known GenesFAM126A
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)nssv6118
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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