A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407031



Internal ID21064584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:124728340..124732022hg38UCSC Ensembl
chr5:124064033..124067715hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg383683
hg193683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18124567
Samples
Known GenesZNF608
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407031
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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