A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18128759



Internal ID20695799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154956085..155074352hg38UCSC Ensembl
chr5:154335645..154453912hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38118268
hg19118268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6403135
Supporting Variants
Samples
Known GenesKIF4B, MRPL22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18128759
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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