A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15740536



Internal ID2073856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75111618..75112178hg38UCSC Ensembl
Innerchr17:75111621..75112176hg38UCSC Ensembl
Outerchr17:75111616..75112181hg38UCSC Ensembl
chr17:73107713..73108273hg19UCSC Ensembl
Innerchr17:73107716..73108271hg19UCSC Ensembl
Outerchr17:73107711..73108276hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38561
hg19561
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641259
Supporting Variants
SamplesHG01885
Known GenesARMC7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15740536
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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