A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2652840



Internal ID17849967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:26960488..26961879hg38UCSC Ensembl
Innerchr17:25287514..25288905hg19UCSC Ensembl
Innerchr17:22311641..22313032hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg381392
hg191392
hg181392
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv962394
Supporting Variants
SamplesHGDP01029
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2652840
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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