A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5025



Internal ID15542865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:143707042..143868142hg38UCSC Ensembl
Outerchr7:143404135..143565235hg19UCSC Ensembl
Outerchr7:143035068..143196168hg18UCSC Ensembl
Outerchr7:142841783..143002883hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38161101
hg19161101
hg18161101
hg17161101
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7408
Supporting Variants
SamplesNA19129
Known GenesCTAGE6, FAM115A, FAM115C, LOC154761
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)nssv5025
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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