A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966861



Internal ID18602090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:93581769..93592216hg38UCSC Ensembl
Innerchr7:93211081..93221528hg19UCSC Ensembl
Innerchr7:93049017..93059464hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3810448
hg1910448
hg1810448
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2469024, nssv2469025, nssv2469022, nssv2469018, nssv2469026, nssv2469017, nssv2469020, nssv2469019, nssv2469023, nssv2469021
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)nsv966861
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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