A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2632778



Internal ID17523239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28337484..28343058hg38UCSC Ensembl
Innerchr16:28348805..28354379hg19UCSC Ensembl
Innerchr16:28256306..28261880hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg385575
hg195575
hg185575
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv984298
Supporting Variants
SamplesHGDP01284
Known GenesNPIPB6
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2632778
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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