A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981127



Internal ID18269640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:30055119..30055963hg38UCSC Ensembl
Innerchr6:30022896..30023740hg19UCSC Ensembl
Innerchr6:30130875..30131719hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38845
hg19845
hg18845
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2402029, nssv2402025, nssv2402028, nssv2402021, nssv2402022, nssv2402024, nssv2402027, nssv2402026, nssv2402023, nssv2402030
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesZNRD1-AS1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981127
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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