A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501824



Internal ID22559763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142061293..142096249hg38UCSC Ensembl
chr6:142382430..142417386hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3834957
hg1934957
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844102
Supporting Variants
Samples
Known GenesNMBR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501824
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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