A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv946713



Internal ID18246877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:148542034..148542534hg38UCSC Ensembl
Innerchr1:144203491..144203991hg19UCSC Ensembl
Innerchr1:142914848..142915348hg18UCSC Ensembl
Cytoband1q21.1
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 Variantsnssv2579969, nssv2580025, nssv2579966, nssv2579964, nssv2579962, nssv2579963, nssv2580027, nssv2579967, nssv2579965, nssv2579960, nssv2580022, nssv2580026, nssv2579961, nssv2580028, nssv2580021, nssv2580019, nssv2580023, nssv2580024, nssv2580020, nssv2579968
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesLOC100288142
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv946713
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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