A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1692



Internal ID15540975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:143727108..143849068hg38UCSC Ensembl
Outerchr7:143424201..143546161hg19UCSC Ensembl
Outerchr7:143055134..143177094hg18UCSC Ensembl
Outerchr7:142861849..142983809hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38121961
hg19121961
hg18121961
hg17121961
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7408
Supporting Variants
SamplesNA18555
Known GenesCTAGE6, 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)nssv1692
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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