A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967821



Internal ID18256363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:28184..71704hg38UCSC Ensembl
Innerchr4:28184..71596hg19UCSC Ensembl
Innerchr4:18184..61596hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3843521
hg1943413
hg1843413
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2691762, nssv2691764, nssv2691771, nssv2691763, nssv2691769, nssv2691766, nssv2691768, nssv2691767, nssv2691770, nssv2691765
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesZNF595, ZNF718
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967821
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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