A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9438



Internal ID15540389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:40806976..40840551hg38UCSC Ensembl
Outerchr7:40846575..40880150hg19UCSC Ensembl
Outerchr7:40813100..40846675hg18UCSC Ensembl
Outerchr7:40619815..40653390hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3833576
hg1933576
hg1833576
hg1733576
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7394
Supporting Variants
SamplesNA18517
Known GenesC7orf10
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)nssv9438
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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