A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966903



Internal ID18255446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143935264..143936264hg38UCSC Ensembl
Innerchr7:143632357..143633357hg19UCSC Ensembl
Innerchr7:143263290..143264290hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg381001
hg191001
hg181001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2483728, nssv2483722, nssv2483724, nssv2483726, nssv2483723, nssv2483720, nssv2483727, nssv2483721, nssv2483725, nssv2483719
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOR2F2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966903
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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