A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059954



Internal ID18802485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:30301334..30339600hg38UCSC Ensembl
Innerchr21:31673652..31711918hg19UCSC Ensembl
Innerchr21:30595523..30633789hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3838267
hg1938267
hg1838267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600114
Samples
Known GenesKRTAP26-1, KRTAP27-1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059954
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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