A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316078



Internal ID20849155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36176201..36179200hg38UCSC Ensembl
chr1:36641802..36644801hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060727
Samples
Known GenesMAP7D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316078
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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