A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982764



Internal ID18271273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:50008912..50011793hg38UCSC Ensembl
Innerchr10:51223380..51226264hg19UCSC Ensembl
Innerchr10:50893386..50896270hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg382882
hg192885
hg182885
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2615011, nssv2615013, nssv2615016, nssv2615015, nssv2615009, nssv2615012, nssv2615014, nssv2615017, nssv2615010, nssv2615008
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesAGAP8, PARG
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982764
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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