A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17158514



Internal ID21403663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43128820..43128964hg38UCSC Ensembl
chr7:43168419..43168563hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5584095
Supporting Variants
SamplesHG00171
Known GenesHECW1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17158514
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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