A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18144586



Internal ID20711626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:81636019..81639329hg38UCSC Ensembl
chr6:82345736..82349046hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg383311
hg193311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415169
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18144586
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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