A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395022



Internal ID21052575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:57144510..57163127hg38UCSC Ensembl
chr4:58010676..58029293hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3818618
hg1918618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117931
Samples
Known GenesIGFBP7-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395022
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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