A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7408



Internal ID15552414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:143561812..143909163hg38UCSC Ensembl
Outerchr7:143258905..143606256hg19UCSC Ensembl
Outerchr7:142969027..143237189hg18UCSC Ensembl
Outerchr7:142775742..143043904hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38347352
hg19347352
hg18268163
hg17268163
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5026, nssv6174, nssv9730, nssv1692, nssv11166, nssv3586, nssv9449, nssv11165, nssv5025, nssv6175
SamplesNA18507, NA12156, NA12878, NA15510, NA18555, NA18517, NA19129
Known GenesCTAGE15, CTAGE6, 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)nsv7408
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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