A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2735384



Internal ID17875056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42857533..42869601hg38UCSC Ensembl
Innerchr9:44101518..44113586hg19UCSC Ensembl
Innerchr9:44041514..44053582hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3812069
hg1912069
hg1812069
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv973634
Supporting Variants
SamplesHGDP01284
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2735384
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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