A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330386



Internal ID20863543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:103836993..104103488hg38UCSC Ensembl
chr1:104379615..104646110hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38266496
hg19266496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050987
Samples
Known GenesLOC100129138
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330386
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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