A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970810



Internal ID18606032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:28278423..28279869hg38UCSC Ensembl
Innerchr7:28318042..28319488hg19UCSC Ensembl
Innerchr7:28284567..28286013hg18UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg381447
hg191447
hg181447
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2439645, nssv2439641, nssv2439650, nssv2439646, nssv2439648, nssv2439644, nssv2439647, nssv2439649, nssv2439643, nssv2439642
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)nsv970810
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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