A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977740



Internal ID18266260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:78802587..78806670hg38UCSC Ensembl
Innerchr15:79094929..79099012hg19UCSC Ensembl
Innerchr15:76881984..76886067hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg384084
hg194084
hg184084
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2032965, nssv2032968, nssv2032967, nssv2032962, nssv2032966, nssv2032970, nssv2032964, nssv2032969, nssv2032971, nssv2032963
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesADAMTS7
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977740
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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