A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981565



Internal ID18270076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:103098107..103099870hg38UCSC Ensembl
Innerchr7:102738554..102740317hg19UCSC Ensembl
Innerchr7:102525790..102527553hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381764
hg191764
hg181764
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2474396, nssv2474394, nssv2474390, nssv2474392, nssv2474391, nssv2474389, nssv2474395, nssv2474393, nssv2474397, nssv2474398
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesARMC10, NAPEPLD
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981565
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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