A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17157511



Internal ID21505535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73600643..73600722hg38UCSC Ensembl
chr7:73014973..73015052hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5577617
Supporting Variants
SamplesNA19650
Known GenesMLXIPL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17157511
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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