A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14250558



Internal ID21308402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:209908268..209910639hg38UCSC Ensembl
Outerchr1:209897717..209913207hg38UCSC Ensembl
Innerchr1:210081613..210083984hg19UCSC Ensembl
Outerchr1:210071062..210086552hg19UCSC Ensembl
Innerchr1:208148236..208150607hg18UCSC Ensembl
Outerchr1:208137685..208153175hg18UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3815491
hg1915491
hg1815491
Variant TypeCNV deletion
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170235
Supporting Variants
SamplesNGO_41
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14250558
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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