A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970803



Internal ID18606025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:22508077..22527358hg38UCSC Ensembl
Innerchr7:22547696..22566977hg19UCSC Ensembl
Innerchr7:22514221..22533502hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3819282
hg1919282
hg1819282
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2438348, nssv2438342, nssv2438343, nssv2438341, nssv2438347, nssv2438346, nssv2438349, nssv2438350, nssv2438344, nssv2438345
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970803
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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