A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17575241



Internal ID21767284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73429187..73432815hg38UCSC Ensembl
chr6:74138910..74142538hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg383629
hg193629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6002499
Supporting Variants
Samples
Known GenesMB21D1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17575241
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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