A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18144797



Internal ID20711837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:57050957..57051661hg38UCSC Ensembl
chr6:56915755..56916459hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38705
hg19705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6413104
Supporting Variants
Samples
Known GenesKIAA1586
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18144797
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01001


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