A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984084



Internal ID18619274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:64590179..64594130hg38UCSC Ensembl
Innerchr15:64882378..64886329hg19UCSC Ensembl
Innerchr15:62669431..62673382hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg383952
hg193952
hg183952
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2028192, nssv2028185, nssv2028187, nssv2028191, nssv2028193, nssv2028188, nssv2028190, nssv2028186, nssv2028189, nssv2028194
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZNF609
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv984084
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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