A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17575882



Internal ID21767925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73836200..73836396hg38UCSC Ensembl
chr7:73250530..73250726hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6014756
Supporting Variants
Samples
Known GenesWBSCR27
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17575882
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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