A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981586



Internal ID18616783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:136937948..136941611hg38UCSC Ensembl
Innerchr7:136622695..136626358hg19UCSC Ensembl
Innerchr7:136273235..136276898hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg383664
hg193664
hg183664
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2479149, nssv2479150, nssv2479147, nssv2479148, nssv2479153, nssv2479151, nssv2479152, nssv2479145, nssv2479146, nssv2479144
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCHRM2, LOC349160
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981586
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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