A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155236



Internal ID21473412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23100260..23104692hg38UCSC Ensembl
chr7:23139879..23144311hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg384433
hg194433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569839
Supporting Variants
SamplesHG03371
Known GenesKLHL7-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155236
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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