A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970997



Internal ID18606219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:39797842..39799704hg38UCSC Ensembl
Innerchr7:39837441..39839303hg19UCSC Ensembl
Innerchr7:39803966..39805828hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg381863
hg191863
hg181863
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2708137, nssv2708135, nssv2708136, nssv2708133, nssv2708131, nssv2708129, nssv2708132, nssv2708128, nssv2708130, nssv2708134
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970997
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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