A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10153172



Internal ID154988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156522172..156526068hg38UCSC Ensembl
Innerchr1:156522172..156526068hg38UCSC Ensembl
Outerchr1:156521940..156526190hg38UCSC Ensembl
chr1:156491964..156495860hg19UCSC Ensembl
Innerchr1:156491964..156495860hg19UCSC Ensembl
Outerchr1:156491732..156495982hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg383897
hg193897
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3587638
Supporting Variants
SamplesHG00334
Known GenesIQGAP3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10153172
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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