A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14249344



Internal ID21303858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140304239..140308666hg38UCSC Ensembl
Outerchr7:140303735..140308668hg38UCSC Ensembl
Innerchr7:140004039..140008466hg19UCSC Ensembl
Outerchr7:140003535..140008468hg19UCSC Ensembl
Innerchr7:139650508..139654935hg18UCSC Ensembl
Outerchr7:139650004..139654937hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg384934
hg194934
hg184934
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170319
Supporting Variants
SamplesMLY_9
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14249344
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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