A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2729118



Internal ID17817513
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 StatusS
Merged Variantsnsv982405
Supporting Variants
SamplesHGDP00927
Known GenesFAM95B1
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2729118
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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