A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2560652



Internal ID17803722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:94348280..94359708hg38UCSC Ensembl
Innerchr9:97110562..97121990hg19UCSC Ensembl
Innerchr9:96150383..96161811hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3811429
hg1911429
hg1811429
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv972422
Supporting Variants
SamplesHGDP00778
Known GenesLOC100132077
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2560652
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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