A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962693



Internal ID18597936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13948553..13949884hg38UCSC Ensembl
Innerchr21:15320874..15322205hg19UCSC Ensembl
Innerchr21:14242745..14244076hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg381332
hg191332
hg181332
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2678617, nssv2678612, nssv2678618, nssv2678614, nssv2678613, nssv2678615, nssv2678611, nssv2678619, nssv2678616, nssv2678620
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A11P
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv962693
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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