A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14249704



Internal ID21306017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:109557461..109635655hg38UCSC Ensembl
Outerchr7:109550778..109648247hg38UCSC Ensembl
Innerchr7:109197518..109275712hg19UCSC Ensembl
Outerchr7:109190835..109288304hg19UCSC Ensembl
Innerchr7:108984754..109062948hg18UCSC Ensembl
Outerchr7:108978071..109075540hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3897470
hg1997470
hg1897470
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170105
Supporting Variants
SamplesNGO_24
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14249704
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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