A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18062330



Internal ID20629370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6383204..6394623hg38UCSC Ensembl
chr1:6443264..6454683hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg3811420
hg1911420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6323179
Supporting Variants
Samples
Known GenesACOT7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18062330
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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