A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704831



Internal ID15094797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35728624..35735098hg38UCSC Ensembl
Innerchr19:36219525..36225999hg19UCSC Ensembl
Innerchr19:40911365..40917839hg18UCSC Ensembl
Innerchr19:40911365..40917839hg17UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg386475
hg196475
hg186475
hg176475
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515536
Supporting Variants
Samples
Known GenesKMT2B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704831
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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