A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978358



Internal ID18613563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:9853037..9854172hg38UCSC Ensembl
Innerchr17:9756354..9757489hg19UCSC Ensembl
Innerchr17:9697079..9698214hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381136
hg191136
hg181136
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2075207, nssv2075208, nssv2075216, nssv2075214, nssv2075210, nssv2075213, nssv2075211, nssv2075209, nssv2075212, nssv2075215
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesGLP2R
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv978358
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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