A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970922



Internal ID18606144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:103164911..103170367hg38UCSC Ensembl
Innerchr7:102805358..102810814hg19UCSC Ensembl
Innerchr7:102592594..102598050hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg385457
hg195457
hg185457
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2473126, nssv2473127, nssv2473123, nssv2473129, nssv2473122, nssv2473125, nssv2473128, nssv2473130, nssv2473124, nssv2473131
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)nsv970922
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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