A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17449071



Internal ID22506941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:70559110..70583270hg38UCSC Ensembl
chr6:71268813..71292973hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3824161
hg1924161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898810
Supporting Variants
Samples
Known GenesC6orf57, FAM135A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17449071
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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