A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981606



Internal ID18616803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149310128..149321460hg38UCSC Ensembl
Innerchr7:149007219..149018551hg19UCSC Ensembl
Innerchr7:148638152..148649484hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3811333
hg1911333
hg1811333
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2486664, nssv2486659, nssv2486663, nssv2486660, nssv2486657, nssv2486662, nssv2486655, nssv2486661, nssv2486658, nssv2486656
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)nsv981606
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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