A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966244



Internal ID18254788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:285652..309350hg38UCSC Ensembl
Innerchr4:279441..303139hg19UCSC Ensembl
Innerchr4:269441..293139hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3823699
hg1923699
hg1823699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2309113, nssv2309118, nssv2309112, nssv2309121, nssv2309117, nssv2309120, nssv2309116, nssv2309114, nssv2309115, nssv2309119
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesZNF732
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966244
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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