A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636735



Internal ID7023529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64520253..64521864hg38UCSC Ensembl
Innerchr15:64520303..64521814hg38UCSC Ensembl
Outerchr15:64520151..64521966hg38UCSC Ensembl
chr15:64812452..64814063hg19UCSC Ensembl
Innerchr15:64812502..64814013hg19UCSC Ensembl
Outerchr15:64812350..64814165hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381612
hg191612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15271631, essv15271630, essv15271633, essv15271632
SamplesHG03378, NA18917, HG03571, HG02759
Known GenesZNF609
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636735
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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