A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323019



Internal ID20856134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56947890..56951788hg38UCSC Ensembl
chr1:57413563..57417461hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg383899
hg193899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062381
Samples
Known GenesC8B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323019
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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