A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2752167



Internal ID12985719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65097016..65603718hg38UCSC Ensembl
Innerchr7:64557394..65068631hg19UCSC Ensembl
Innerchr7:64194829..64706066hg18UCSC Ensembl
Innerchr7:64001544..64512781hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38506703
hg19511238
hg18511238
hg17511238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv227e55
Supporting Variantsessv6985257, essv6990102, essv6985258, essv6989484
SamplesSPC_13
Known GenesZNF92
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2752167
Frequency
Sample Size771
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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