A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7043



Internal ID15536821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:155346096..155377860hg38UCSC Ensembl
Outerchr3:155063885..155095649hg19UCSC Ensembl
Outerchr3:156546579..156578343hg18UCSC Ensembl
Outerchr3:156546587..156578351hg17UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg387662
hg197662
hg187662
hg177662
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4075
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)nssv7043
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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