A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16079953



Internal ID5166945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51576239..51577757hg38UCSC Ensembl
Innerchr19:51576303..51577693hg38UCSC Ensembl
Outerchr19:51576175..51577821hg38UCSC Ensembl
chr19:52079492..52081010hg19UCSC Ensembl
Innerchr19:52079556..52080946hg19UCSC Ensembl
Outerchr19:52079428..52081074hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg381519
hg191519
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644673
Supporting Variants
SamplesNA18596
Known GenesZNF175
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16079953
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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