A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977803



Internal ID18266323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84177398..84205093hg38UCSC Ensembl
Innerchr15:84846150..84873845hg19UCSC Ensembl
Innerchr15:82637154..82664849hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3827696
hg1927696
hg1827696
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2626803, nssv2626800, nssv2626805, nssv2626799, nssv2626804, nssv2626807, nssv2626801, nssv2626802, nssv2626806, nssv2626798
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesLOC100505679, LOC388152, LOC440300, LOC642423
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977803
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer