A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9724



Internal ID15539977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:104796293..104845378hg38UCSC Ensembl
Outerchr7:104436740..104485825hg19UCSC Ensembl
Outerchr7:104223976..104273061hg18UCSC Ensembl
Outerchr7:104030691..104079776hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3849086
hg1949086
hg1849086
hg1749086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5887
Supporting Variants
SamplesNA18507
Known GenesLHFPL3, LHFPL3-AS1
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)nssv9724
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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