A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970834



Internal ID18606056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55634976..55642359hg38UCSC Ensembl
Innerchr7:55702669..55710052hg19UCSC Ensembl
Innerchr7:55670163..55677546hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg387384
hg197384
hg187384
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2446743, nssv2446739, nssv2446737, nssv2446744, nssv2446741, nssv2446738, nssv2446746, nssv2446745, nssv2446742, nssv2446740
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970834
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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