A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982753



Internal ID18271262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46367929..46374529hg38UCSC Ensembl
Innerchr10:47176239..47182846hg19UCSC Ensembl
Innerchr10:46596245..46602852hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg386601
hg196608
hg186608
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2612799, nssv2612803, nssv2612795, nssv2612801, nssv2612794, nssv2612796, nssv2612802, nssv2612798, nssv2612797, nssv2612800
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFAM25C, FAM25G
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982753
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer