A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614063



Internal ID6654270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:88966558..88970927hg38UCSC Ensembl
Innerchr7:88966562..88970923hg38UCSC Ensembl
Outerchr7:88966554..88970931hg38UCSC Ensembl
chr7:88595872..88600241hg19UCSC Ensembl
Innerchr7:88595876..88600237hg19UCSC Ensembl
Outerchr7:88595868..88600245hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg384370
hg194370
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12881169, essv12881168
SamplesHG03756, NA19723
Known GenesZNF804B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614063
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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