A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057557



Internal ID18800088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59857564..59924573hg38UCSC Ensembl
Innerchr20:58432619..58499628hg19UCSC Ensembl
Innerchr20:57866014..57933023hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3867010
hg1967010
hg1867010
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4336n100
Supporting Variantsnssv3584277, nssv3584273, nssv3584274, nssv3584275, nssv3584276
Samples
Known GenesSYCP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057557
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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