A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981551



Internal ID18270062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:97851965..97853571hg38UCSC Ensembl
Innerchr7:97481277..97482883hg19UCSC Ensembl
Innerchr7:97319213..97320819hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg381607
hg191607
hg181607
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2470356, nssv2470358, nssv2470357, nssv2470351, nssv2470355, nssv2470350, nssv2470352, nssv2470349, nssv2470353, nssv2470354
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesASNS
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981551
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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