A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316926



Internal ID20850008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:82750256..82750803hg38UCSC Ensembl
chr1:83215939..83216486hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38548
hg19548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064839
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316926
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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