A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7108



Internal ID15536756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:96975096..97007344hg38UCSC Ensembl
Outerchr4:97896247..97928495hg19UCSC Ensembl
Outerchr4:98115270..98147518hg18UCSC Ensembl
Outerchr4:98253425..98285673hg17UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg387186
hg197186
hg187186
hg177186
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434
Supporting Variants
SamplesNA12156
Known Genes
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)nssv7108
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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