A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2626817



Internal ID17503005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84205093..84206783hg38UCSC Ensembl
Innerchr15:84873845..84875535hg19UCSC Ensembl
Innerchr15:82664849..82666539hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg381691
hg191691
hg181691
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv984148
Supporting Variants
SamplesHGDP01029
Known GenesLOC388152, LOC440300
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2626817
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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