A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439595



Internal ID22497465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73444243..73444563hg38UCSC Ensembl
chr6:74153966..74154286hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5893914
Supporting Variants
Samples
Known GenesMB21D1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439595
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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