A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970162



Internal ID18258700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:126480556..126498274hg38UCSC Ensembl
Innerchr6:126801702..126819420hg19UCSC Ensembl
Innerchr6:126843395..126861113hg18UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg3817719
hg1917719
hg1817719
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2422617, nssv2422611, nssv2422616, nssv2422612, nssv2422613, nssv2422615, nssv2422618, nssv2422614, nssv2422619, nssv2422620
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCENPW
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970162
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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