A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977286



Internal ID18265806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18848373..18848873hg38UCSC Ensembl
Innerchr13:19422513..19423013hg19UCSC Ensembl
Innerchr13:18320513..18321013hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2618836, nssv2618835, nssv2618838, nssv2618840, nssv2618842, nssv2618837, nssv2618839, nssv2618844, nssv2618843, nssv2618841
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesANKRD20A9P
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977286
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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