A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961379



Internal ID18596625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:9269449..9274669hg38UCSC Ensembl
Innerchr2:9409578..9414798hg19UCSC Ensembl
Innerchr2:9327029..9332249hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg385221
hg195221
hg185221
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2166147, nssv2166144, nssv2166149, nssv2166148, nssv2166143, nssv2166142, nssv2166150, nssv2166151, nssv2166146, nssv2166145
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesASAP2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv961379
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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