A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970153



Internal ID18605377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:96648381..96649146hg38UCSC Ensembl
Innerchr6:97096257..97097022hg19UCSC Ensembl
Innerchr6:97202978..97203743hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38766
hg19766
hg18766
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2418302, nssv2417771, nssv2418304, nssv2418301, nssv2417770, nssv2418300, nssv2417768, nssv2418305, nssv2418303, nssv2417769
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)nsv970153
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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