A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15198098



Internal ID21336894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73836551..73836629hg38UCSC Ensembl
chr7:73250881..73250959hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3950553
Supporting Variants
SamplesHG002
Known GenesWBSCR27
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15198098
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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