A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968697



Internal ID18603925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65762114..65768709hg38UCSC Ensembl
Innerchr9:70397336..70403931hg19UCSC Ensembl
Innerchr9:69637156..69643751hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg386596
hg196596
hg186596
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2748861, nssv2747404, nssv2754186, nssv2754543, nssv2751956, nssv2751547, nssv2753103, nssv2747843, nssv2752890, nssv2752744, nssv2756423, nssv2750470, nssv2752198, nssv2755533, nssv2750317, nssv2751819, nssv2753776, nssv2751077, nssv2755488, nssv2747726
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)nsv968697
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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