A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970075



Internal ID18605299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:5829037..5841281hg38UCSC Ensembl
Innerchr6:5829270..5841514hg19UCSC Ensembl
Innerchr6:5774269..5786513hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3812245
hg1912245
hg1812245
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2393290, nssv2392755, nssv2393286, nssv2393285, nssv2392757, nssv2393289, nssv2393288, nssv2392756, nssv2393287, nssv2392754
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)nsv970075
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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