A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981488



Internal ID18616685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:61071607..61074006hg38UCSC Ensembl
Innerchr7:61054332..61056731hg19UCSC Ensembl
Innerchr7:61058085..61060673hg18UCSC Ensembl
Cytoband7q11.1
Allele length
AssemblyAllele length
hg382400
hg192400
hg182589
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv76n82
Supporting Variantsnssv2711673, nssv2711665, nssv2711669, nssv2711674, nssv2711672, nssv2711667, nssv2711666, nssv2711670, nssv2711668, nssv2711671
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981488
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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