A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326532



Internal ID20859668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:96118701..96119600hg38UCSC Ensembl
chr1:96584257..96585156hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065291
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326532
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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