A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379014



Internal ID21036567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:147737926..147738197hg38UCSC Ensembl
chr4:148659077..148659348hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18109614
Samples
Known GenesARHGAP10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379014
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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