A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970176



Internal ID18258714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149998037..150022193hg38UCSC Ensembl
Innerchr6:150319173..150343329hg19UCSC Ensembl
Innerchr6:150360866..150385022hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3824157
hg1924157
hg1824157
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2428541, nssv2428540, nssv2428538, nssv2428544, nssv2428539, nssv2428536, nssv2428545, nssv2428543, nssv2428542, nssv2428537
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRAET1K, RAET1L
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970176
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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