A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982405



Internal ID18617600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:40326297..40332941hg38UCSC Ensembl
Innerchr9:42471315..42477959hg19UCSC Ensembl
Innerchr9:42461311..42467955hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg386645
hg196645
hg186645
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2729114, nssv2729112, nssv2729111, nssv2729113, nssv2729109, nssv2729118, nssv2729110, nssv2729116, nssv2729117, nssv2729115
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFAM95B1
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982405
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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