A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350175



Internal ID21007728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:135622974..135623574hg38UCSC Ensembl
chr2:136380544..136381144hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18077898
Samples
Known GenesR3HDM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350175
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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