A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966904



Internal ID18602133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144434201..144435457hg38UCSC Ensembl
Innerchr7:144131294..144132550hg19UCSC Ensembl
Innerchr7:143762227..143763483hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg381257
hg191257
hg181257
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2485688, nssv2485686, nssv2485693, nssv2485685, nssv2485689, nssv2485694, nssv2485687, nssv2485691, nssv2485690, nssv2485692
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)nsv966904
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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