A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352830



Internal ID21010383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:74638166..74641957hg38UCSC Ensembl
chr2:74865293..74869084hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg383792
hg193792
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090221
Samples
Known GenesM1AP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352830
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer