A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970621



Internal ID18605843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:156620666..156635709hg38UCSC Ensembl
Innerchr7:156413360..156428403hg19UCSC Ensembl
Innerchr7:156106121..156121164hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3815044
hg1915044
hg1815044
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2490774, nssv2490776, nssv2490770, nssv2490773, nssv2490772, nssv2490767, nssv2490769, nssv2490775, nssv2490771, nssv2490768
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)nsv970621
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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