A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976772



Internal ID18611978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:84173076..84175278hg38UCSC Ensembl
Innerchr14:84639420..84641622hg19UCSC Ensembl
Innerchr14:83709173..83711375hg18UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg382203
hg192203
hg182203
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2623009, nssv2623016, nssv2623010, nssv2623015, nssv2623018, nssv2623017, nssv2623013, nssv2623014, nssv2623011, nssv2623012
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976772
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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