A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2727473



Internal ID17762924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39855436..39861438hg38UCSC Ensembl
Innerchr9:42000454..42006456hg19UCSC Ensembl
Innerchr9:41990454..41996456hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg386003
hg196003
hg186003
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv973239
Supporting Variants
SamplesHGDP00542
Known GenesKGFLP2, LOC643648
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2727473
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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