A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316735



Internal ID20849816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:219690301..219691000hg38UCSC Ensembl
chr1:219863643..219864342hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057837
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316735
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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