A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13039917



Internal ID3041733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156841904..156842444hg38UCSC Ensembl
Innerchr7:156841904..156842444hg38UCSC Ensembl
Outerchr7:156841455..156842832hg38UCSC Ensembl
chr7:156634598..156635138hg19UCSC Ensembl
Innerchr7:156634598..156635138hg19UCSC Ensembl
Outerchr7:156634149..156635526hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38541
hg19541
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3615679
Supporting Variants
SamplesHG01356
Known GenesLMBR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13039917
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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