A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970807



Internal ID18259343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:26184557..26186155hg38UCSC Ensembl
Innerchr7:26224177..26225775hg19UCSC Ensembl
Innerchr7:26190702..26192300hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg381599
hg191599
hg181599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2440433, nssv2440434, nssv2440428, nssv2440427, nssv2440435, nssv2440430, nssv2440432, nssv2440431, nssv2440429, nssv2440426
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesNFE2L3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970807
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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