A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403135



Internal ID21060688
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 StatusM
Merged Variants
Supporting Variantsnssv18128759
Samples
Known GenesKIF4B, MRPL22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403135
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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